rs1800562

Homo sapiens
G>A
HFE : Missense Variant
Check p-value
SNV (Single Nucleotide Variation)
A=0032 (3937/121394,ExAC)
A=0037 (1131/29944,GnomAD)
A=0031 (928/29118,TOPMED)
A=0013 (63/5008,1000G)
A=0079 (306/3854,ALSPAC)
A=0069 (256/3708,TWINSUK)
chr6:26092913 (GRCh38.p7) (6p22.2)
AD
GWASdb2
See rs on genome

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.26092913G>A
GRCh37.p13 chr 6NC_000006.11:g.26093141G>A
HFE RefSeqGene LRG_748

Gene: HFE, hemochromatosis(plus strand)

Molecule type Change Amino acid[Codon] SO Term
HFE transcript variant 11NM_139011.2:c.N/AIntron Variant
HFE transcript variant 1NM_000410.3:c.845G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 1 precursorNP_000401.1:p.Cys...NP_000401.1:p.Cys282TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 3NM_139003.2:c.527G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 3 precursorNP_620572.1:p.Cys...NP_620572.1:p.Cys176TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 4NM_139004.2:c.569G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 4 precursorNP_620573.1:p.Cys...NP_620573.1:p.Cys190TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 6NM_139006.2:c.803G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 6 precursorNP_620575.1:p.Cys...NP_620575.1:p.Cys268TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 7NM_139007.2:c.581G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 7 precursorNP_620576.1:p.Cys...NP_620576.1:p.Cys194TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 8NM_139008.2:c.539G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 8 precursorNP_620577.1:p.Cys...NP_620577.1:p.Cys180TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 9NM_139009.2:c.776G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 9 precursorNP_620578.1:p.Cys...NP_620578.1:p.Cys259TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 10NM_139010.2:c.305G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 10 precursorNP_620579.1:p.Cys...NP_620579.1:p.Cys102TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant 12NM_001300749.1:c....NM_001300749.1:c.845G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform 12 precursorNP_001287678.1:p....NP_001287678.1:p.Cys282TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant X1XM_011514543.2:c....XM_011514543.2:c.845G>AC [TGC]> Y [TAC]Coding Sequence Variant
hereditary hemochromatosis protein isoform X1XP_011512845.1:p....XP_011512845.1:p.Cys282TyrC [Cys]> Y [Tyr]Missense Variant
HFE transcript variant X2XR_241893.3:n.967G>AG>ANon Coding Transcript Variant

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.998A=0.002
1000GenomesAmericanSub694G=0.980A=0.020
1000GenomesEast AsianSub1008G=1.000A=0.000
1000GenomesEuropeSub1006G=0.957A=0.043
1000GenomesGlobalStudy-wide5008G=0.987A=0.013
1000GenomesSouth AsianSub978G=1.000A=0.000
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.921A=0.079
The Exome Aggregation ConsortiumAmericanSub21978G=0.989A=0.010
The Exome Aggregation ConsortiumAsianSub25166G=0.998A=0.001
The Exome Aggregation ConsortiumEuropeSub73342G=0.950A=0.049
The Exome Aggregation ConsortiumGlobalStudy-wide121394G=0.967A=0.032
The Exome Aggregation ConsortiumOtherSub908G=0.980A=0.020
The Genome Aggregation DatabaseAfricanSub8716G=0.990A=0.010
The Genome Aggregation DatabaseAmericanSub832G=0.970A=0.030
The Genome Aggregation DatabaseEast AsianSub1620G=0.999A=0.001
The Genome Aggregation DatabaseEuropeSub18474G=0.945A=0.054
The Genome Aggregation DatabaseGlobalStudy-wide29944G=0.962A=0.037
The Genome Aggregation DatabaseOtherSub302G=0.980A=0.020
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.968A=0.031
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.931A=0.069
PMID Title Author Journal
24926413Design and implementation of a randomized controlled trial of genomic counseling for patients with chronic disease.Sweet KJ Pers Med
21452290Diagnosis and management of hemochromatosis: 2011 practice guideline by the American Association for the Study of Liver Diseases.Bacon BRHepatology
22408404Molecular diagnostic and pathogenesis of hereditary hemochromatosis.Santos PCInt J Mol Sci
23468552Genetic variants influencing biomarkers of nutrition are not associated with cognitive capability in middle-aged and older adults.Alfred TJ Nutr
19444013HFE-associated hereditary hemochromatosis.Alexander JGenet Med
27547017Genetic factors that affect nonalcoholic fatty liver disease: A systematic clinical review.Severson TJWorld J Gastroenterol
21483845Genome-wide association study identifies genetic loci associated with iron deficiency.McLaren CEPLoS One
18795173Variants in iron metabolism genes predict higher blood lead levels in young children.Hopkins MREnviron Health Perspect
27280446Replication and Characterization of Association between ABO SNPs and Red Blood Cell Traits by Meta-Analysis in Europeans.McLachlan SPLoS One
8896550Haemochromatosis and HLA-H.Jouanolle AMNat Genet
9024376Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda.Roberts AGLancet
9211748Absence of the hemochromatosis gene Cys282Tyr mutation in three ethnic groups from Algeria (Mzab), Ethiopia, and Senegal.Roth MImmunogenetics
27657935Association between the HFE C282Y, H63D Polymorphisms and the Risks of Non-Alcoholic Fatty Liver Disease, Liver Cirrhosis and Hepatocellular Carcinoma: An Updated Systematic Review and Meta-Analysis of 5,758 Cases and 14,741 Controls.Ye QPLoS One
12436244Hereditary haemochromatosis: only 1% of adult HFEC282Y homozygotes in South Wales have a clinical diagnosis of iron overload.McCune CAHum Genet
26025379Genome-wide association study of toxic metals and trace elements reveals novel associations.Ng EHum Mol Genet
12429850The hemochromatosis protein HFE inhibits iron export from macrophages.Drakesmith HProc Natl Acad Sci U S A
26695521Mendelian Randomization - the Key to Understanding Aspects of Parkinson's Disease Causation?Noyce AJMov Disord
25302496Using multivariable Mendelian randomization to disentangle the causal effects of lipid fractions.Burgess SPLoS One
25071582HFE gene variants, iron, and lipids: a novel connection in Alzheimer's disease.Ali-Rahmani FFront Pharmacol
18603647Functional genetic polymorphisms and female reproductive disorders: Part I: Polycystic ovary syndrome and ovarian response.Simoni MHum Reprod Update
21138591Effect modification of air pollution on Urinary 8-Hydroxy-2'-Deoxyguanosine by genotypes: an application of the multiple testing procedure to identify significant SNP interactions.Ren CEnviron Health
20659343HFE gene variants modify the association between maternal lead burden and infant birthweight: a prospective birth cohort study in Mexico City, Mexico.Cantonwine DEnviron Health
24033266A systematic approach to assessing the clinical significance of genetic variants.Duzkale HClin Genet
22047634The Alzheimer's Disease Neuroimaging Initiative: a review of papers published since its inception.Weiner MWAlzheimers Dement
14618419A hemochromatosis-causing mutation C282Y is a risk factor for proliferative diabetic retinopathy in Caucasians with type 2 diabetes.Peterlin BJ Hum Genet
19401444Body iron stores and glucose intolerance in premenopausal women: role of hyperandrogenism, insulin resistance, and genomic variants related to inflammation, oxidative stress, and iron metabolism.Martinez-Garcia MADiabetes Care
9356458Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cells.Waheed AProc Natl Acad Sci U S A
9439654Phenotype-genotype correlation in haemochromatosis subjects.Mura CHum Genet
19159930Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants.Pedersen PAnn Hematol
21400687Disease and phenotype data at Ensembl.Spudich GMCurr Protoc Hum Genet
22735619Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis.Nielsen PBGene
10401000Spectrum of mutations in the HFE gene implicated in haemochromatosis and porphyria.de Villiers JNHum Mol Genet
21862702Mechanisms and genetic determinants regulating sterol absorption, circulating LDL levels, and sterol elimination: implications for classification and disease risk.Calandra SJ Lipid Res
27846281Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.Galesloot TEPLoS One
26632894Association of ABO and Colton Blood Group Gene Polymorphisms With Hematological Traits Variation.Shahbazi SMedicine (Baltimore)
27584680Lead-Related Genetic Loci, Cumulative Lead Exposure and Incident Coronary Heart Disease: The Normative Aging Study.Ding NPLoS One
19474294Potential etiologic and functional implications of genome-wide association loci for human diseases and traits.Hindorff LAProc Natl Acad Sci U S A
18499578Iron-overload-related disease in HFE hereditary hemochromatosis.Waalen JN Engl J Med
26416403HFE p.C282Y gene variant is associated with varicose veins in Russian population.Sokolova EAClin Exp Med
19862010Multiple loci influence erythrocyte phenotypes in the CHARGE Consortium.Ganesh SKNat Genet
18199861Iron-overload-related disease in HFE hereditary hemochromatosis.Allen KJN Engl J Med
21153663Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans.Lo KSHum Genet
23389292Hemochromatosis (HFE) gene mutations and risk of gastric cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC) study.Agudo ACarcinogenesis
20927387A genome-wide association study of red blood cell traits using the electronic medical record.Kullo IJPLoS One
678784Proliferative retinopathy in a patient with diabetes mellitus and idiopathic haemochromatosis.Walsh CHBr Med J
21208937Identification of a common variant in the TFR2 gene implicated in the physiological regulation of serum iron levels.Pichler IHum Mol Genet
25741868Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.Richards SGenet Med
11040194Differential HFE allele expression in hemochromatosis heterozygotes.Rosmorduc OGastroenterology
21978626Four variants in transferrin and HFE genes as potential markers of iron deficiency anaemia risk: an association study in menstruating women.Blanco-Rojo RNutr Metab (Lond)
23996192Toenail iron, genetic determinants of iron status, and the risk of glioma.Anic GMCancer Causes Control
27317329Haplotype analysis of the HFE gene among populations of Northern Eurasia, in patients with metabolic disorders or stomach cancer, and in long-lived people.Mikhailova SVBMC Genet
21149283Novel association to the proprotein convertase PCSK7 gene locus revealed by analysing soluble transferrin receptor (sTfR) levels.Oexle KHum Mol Genet
23386860Exploring genome-wide - dietary heme iron intake interactions and the risk of type 2 diabetes.Pasquale LRFront Genet
19165391Iron metabolism genes, low-level lead exposure, and QT interval.Park SKEnviron Health Perspect
15280838Association of porphyria cutanea tarda with hereditary hemochromatosis.Mehrany KJ Am Acad Dermatol
23794717Associations of common variants in HFE and TMPRSS6 with iron parameters are independent of serum hepcidin in a general population: a replication study.Galesloot TEJ Med Genet
21785125Association of HFE and TMPRSS6 genetic variants with iron and erythrocyte parameters is only in part dependent on serum hepcidin concentrations.Traglia MJ Med Genet
8896549Haemochromatosis and HLA-H.Jazwinska ECNat Genet
22234866Evidence from case-control and longitudinal studies supports associations of genetic variation in APOE, CETP, and IL6 with human longevity.Soerensen MAge (Dordr)
22815867Genetic determinants for body iron store and type 2 diabetes risk in US men and women.He MPLoS One
18504828Iron-overload-related disease in HFE hereditary hemochromatosis.Rienhoff HY JrN Engl J Med
10431233Polymorphism in intron 4 of HFE may cause overestimation of C282Y homozygote prevalence in haemochromatosis.Jeffrey GPNat Genet
23446634Genome-wide association analysis of red blood cell traits in African Americans: the COGENT Network.Chen ZHum Mol Genet
24398642Maternal iron levels early in pregnancy are not associated with offspring IQ score at age 8, findings from a Mendelian randomization study.Lewis SJEur J Clin Nutr
22074419Associations of iron metabolism genes with blood manganese levels: a population-based study with validation data from animal models.Claus Henn BEnviron Health
21240526Evaluation of the association studies of single nucleotide polymorphisms and hepatocellular carcinoma: a systematic review.Jin FJ Cancer Res Clin Oncol
24121126Pooled analysis of iron-related genes in Parkinson's disease: association with transferrin.Rhodes SLNeurobiol Dis
26460247Genetic contribution to iron status: SNPs related to iron deficiency anaemia and fine mapping of CACNA2D3 calcium channel subunit.Baeza-Richer CBlood Cells Mol Dis
27124787Highly accurate molecular genetic testing for HFE hereditary hemochromatosis: results from 10 years of blinded proficiency surveys by the College of American Pathologists.Press RDGenet Med
19880490A genome-wide association analysis of serum iron concentrations.Tanaka TBlood
25287020Maternal iron metabolism gene variants modify umbilical cord blood lead levels by gene-environment interaction: a birth cohort study.Karwowski MPEnviron Health
20029940Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease.Kauwe JSAm J Med Genet B Neuropsychiatr Genet
16879202Frequency of the hemochromatosis gene mutations in the population of Serbia and Montenegro.Saric MClin Genet
8696333A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis.Feder JNNat Genet
20301613HFE-Associated Hereditary HemochromatosisSeckington R-
15060098Synergy between the C2 allele of transferrin and the C282Y allele of the haemochromatosis gene (HFE) as risk factors for developing Alzheimer's disease.Robson KJJ Med Genet
20556870CLIA-tested genetic variants on commercial SNP arrays: potential for incidental findings in genome-wide association studies.Johnson ADGenet Med
15347835The HFE gene is associated to an earlier age of onset and to the presence of diabetic nephropathy in diabetes mellitus type 2.Oliva REndocrine
18414213ACMG recommendations for standards for interpretation and reporting of sequence variations: Revisions 2007.Richards CSGenet Med
19879291Environmental manganese exposure in residents living near a ferromanganese refinery in Southeast Ohio: a pilot study.Haynes ENNeurotoxicology
27255824Determinants of iron accumulation in the normal aging brain.Pirpamer LNeurobiol Aging
20858683Common variants at 10 genomic loci influence hemoglobin A(1)(C) levels via glycemic and nonglycemic pathways.Soranzo NDiabetes
9341868A candidate gene for hemochromatosis: frequency of the C282Y and H63D mutations.Jouanolle AMHum Genet
8943161Clinical and biochemical abnormalities in people heterozygous for hemochromatosis.Bulaj ZJN Engl J Med
26597663Genetic factors influencing ferritin levels in 14,126 blood donors: results from the Danish Blood Donor Study.Sorensen ETransfusion
24270849Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data.Denny JCNat Biotechnol
26582562Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver.Engelken JMol Biol Evol
21975967Genetic determinants of variability in glycated hemoglobin (HbA(1c)) in humans: review of recent progress and prospects for use in diabetes care.Soranzo NCurr Diab Rep
10381492The C282Y mutation causing hereditary hemochromatosis does not produce a null allele.Levy JEBlood
21860704Implications of discoveries from genome-wide association studies in current cardiovascular practice.Jeemon PWorld J Cardiol
14729817The 16189 variant of mitochondrial DNA occurs more frequently in C282Y homozygotes with haemochromatosis than those without iron loading.Livesey KJJ Med Genet
9585606The hemochromatosis 845 G-->A and 187 C-->G mutations: prevalence in non-Caucasian populations.Cullen LMAm J Hum Genet
22611049Lower serum hepcidin and greater parenchymal iron in nonalcoholic fatty liver disease patients with C282Y HFE mutations.Nelson JEHepatology
9321765Homozygosity for the predominant Cys282Tyr mutation and absence of disease expression in hereditary haemochromatosis.Rhodes DAJ Med Genet
27221532Population-based analysis of the frequency of HFE gene polymorphisms: Correlation with the susceptibility to develop hereditary hemochromatosis.Katsarou MSMol Med Rep
26365338Penetrance of Hemochromatosis in HFE Genotypes Resulting in p.Cys282Tyr and p.[Cys282Tyr];[His63Asp] in the eMERGE Network.Gallego CJAm J Hum Genet
19084217Variants in TF and HFE explain approximately 40% of genetic variation in serum-transferrin levels.Benyamin BAm J Hum Genet
23935582Effects of hemochromatosis and transferrin gene mutations on peripheral iron dyshomeostasis in mild cognitive impairment and Alzheimer's and Parkinson's diseases.Mariani SFront Aging Neurosci
27661980The D519G Polymorphism of Glyceronephosphate O-Acyltransferase Is a Risk Factor for Familial Porphyria Cutanea Tarda.Farrell CPPLoS One
26054392Natural selection on HFE in Asian populations contributes to enhanced non-heme iron absorption.Ye KBMC Genet
25933217Correction: A Systems Genetics Approach Identifies CXCL14, ITGAX, and LPCAT2 as Novel Aggressive Prostate Cancer Susceptibility Genes.-PLoS Genet
23792061Meta-analyses of HFE variants in coronary heart disease.Lian JGene
9162021The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expression.Feder JNJ Biol Chem
19884647Air pollution, obesity, genes and cellular adhesion molecules.Madrigano JOccup Environ Med
8931958Mutation analysis in hereditary hemochromatosis.Beutler EBlood Cells Mol Dis
9138148Global prevalence of putative haemochromatosis mutations.Merryweather-Clarke ATJ Med Genet
21067572Association analysis of nine candidate gene polymorphisms in Indian patients with type 2 diabetic retinopathy.Balasubbu SBMC Med Genet
18566337Prevalence, characteristics, and prognostic significance of HFE gene mutations in type 2 diabetes: the Fremantle Diabetes Study.Davis TMDiabetes Care
11812557Penetrance of 845G--> A (C282Y) HFE hereditary haemochromatosis mutation in the USA.Beutler ELancet
19820699Common variants in TMPRSS6 are associated with iron status and erythrocyte volume.Benyamin BNat Genet
19820698Genome-wide association study identifies variants in TMPRSS6 associated with hemoglobin levels.Chambers JCNat Genet
9851897Celtic origin of the C282Y mutation of hemochromatosis.Lucotte GBlood Cells Mol Dis
9851896Hemochromatosis in Ireland and HFE.Ryan EBlood Cells Mol Dis
15070663Hemochromatosis mutations in the general population: iron overload progression rate.Andersen RVBlood
12241803Clinical haemochromatosis in HFE mutation carriers.Poullis ALancet
23820649Where genotype is not predictive of phenotype: towards an understanding of the molecular basis of reduced penetrance in human inherited disease.Cooper DNHum Genet
19820697A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium.Soranzo NNat Genet
19673882A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.Constantine CCBr J Haematol
26420954Molecular prognostic prediction in liver cirrhosis.Goossens NWorld J Gastroenterol
20846924Altered cardiac repolarization in association with air pollution and air temperature among myocardial infarction survivors.Hampel REnviron Health Perspect
10673304Incidence of liver disease in people with HFE mutations.Willis GGut
24931982GRASP: analysis of genotype-phenotype results from 1390 genome-wide association studies and corresponding open access database.Leslie RBioinformatics
15858186Hemochromatosis and iron-overload screening in a racially diverse population.Adams PCN Engl J Med
20110814Air pollution and homocysteine: more evidence that oxidative stress-related genes modify effects of particulate air pollution.Ren CEpidemiology
19554541HFE C282Y/H63D compound heterozygotes are at low risk of hemochromatosis-related morbidity.Gurrin LCHepatology
22540250Race-ethnic differences in the association of genetic loci with HbA1c levels and mortality in U.S. adults: the third National Health and Nutrition Examination Survey (NHANES III).Grimsby JLBMC Med Genet
12915468Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis.Merryweather-Clarke ATHum Mol Genet
24922540Genetic determinants of long-term changes in blood lipid concentrations: 10-year follow-up of the GLACIER study.Varga TVPLoS Genet
9462220A simple genetic test identifies 90% of UK patients with haemochromatosis. The UK Haemochromatosis Consortium.-Gut
21665994Genome-wide association study identifies two loci strongly affecting transferrin glycosylation.Kutalik ZHum Mol Genet
26159428Iron and hepcidin as risk factors in atherosclerosis: what do the genes say?Galesloot TEBMC Genet
21679129Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000(R) instrument.Santos PCClin Chem Lab Med

P-Value

SNP ID p-value Traits Study
rs18005622E-32alcohol consumption (transferrin glycosylation)21665994

eQTL of rs1800562 in Brain tissues (GTEx Analysis Release V7)

Position (v37) eGene GeneID Variant p-value TSS Tissue
There is no eQTL annotation for this SNP

meQTL of rs1800562 in Fetal Brain

Probe ID Position Gene beta p-value
There is no meQTL annotation for this SNP

Genomic View

Chromatin Interaction

There is no significant Hi-C chromatin interaction data for this SNP.

Enhancer Annotation (GRCh37.p13)

Chromosome Start End Region Distance ( -/+ : Up/Downstream )
chr62612803326128083E06734892
chr62612825226128378E06735111
chr62612977726129821E06736636
chr62612996726130171E06736826
chr62613017926130425E06737038
chr62613051426130656E06737373
chr62614034226140441E06747201
chr62614052126140673E06747380
chr62614089926141510E06747758
chr62614163726141810E06748496
chr62614182626142094E06748685
chr62614236126142495E06749220
chr62614269226142800E06749551
chr62614298226143055E06749841
chr62608966726089831E068-3310
chr62611760926117697E06824468
chr62611886326118940E06825722
chr62612803326128083E06834892
chr62612825226128378E06835111
chr62612842026128913E06835279
chr62612899426129044E06835853
chr62612977726129821E06836636
chr62612996726130171E06836826
chr62613017926130425E06837038
chr62613051426130656E06837373
chr62613094126131475E06837800
chr62613162426131707E06838483
chr62613171426131783E06838573
chr62613190126132235E06838760
chr62613224526132303E06839104
chr62613239026132718E06839249
chr62613397626134065E06840835
chr62614034226140441E06847201
chr62614052126140673E06847380
chr62614089926141510E06847758
chr62614236126142495E06849220
chr62614269226142800E06849551
chr62614298226143055E06849841
chr62611760926117697E06924468
chr62611886326118940E06925722
chr62612803326128083E06934892
chr62612825226128378E06935111
chr62612842026128913E06935279
chr62612899426129044E06935853
chr62613094126131475E06937800
chr62613162426131707E06938483
chr62613171426131783E06938573
chr62614052126140673E06947380
chr62614089926141510E06947758
chr62614236126142495E06949220
chr62614269226142800E06949551
chr62614298226143055E06949841
chr62605405026054116E070-39025
chr62611760926117697E07124468
chr62611886326118940E07125722
chr62611929226119516E07126151
chr62612977726129821E07136636
chr62612996726130171E07136826
chr62613017926130425E07137038
chr62613051426130656E07137373
chr62613094126131475E07137800
chr62613162426131707E07138483
chr62613171426131783E07138573
chr62613190126132235E07138760
chr62613397626134065E07140835
chr62613677926136894E07143638
chr62614034226140441E07147201
chr62614052126140673E07147380
chr62614089926141510E07147758
chr62614236126142495E07149220
chr62614269226142800E07149551
chr62614298226143055E07149841
chr62612803326128083E07234892
chr62612825226128378E07235111
chr62612842026128913E07235279
chr62612899426129044E07235853
chr62612996726130171E07236826
chr62613017926130425E07237038
chr62613051426130656E07237373
chr62613094126131475E07237800
chr62613162426131707E07238483
chr62613171426131783E07238573
chr62613190126132235E07238760
chr62614052126140673E07247380
chr62614089926141510E07247758
chr62614182626142094E07248685
chr62614236126142495E07249220
chr62614269226142800E07249551
chr62614298226143055E07249841
chr62612977726129821E07336636
chr62612996726130171E07336826
chr62613017926130425E07337038
chr62613677926136894E07343638
chr62614163726141810E07348496
chr62614182626142094E07348685
chr62614236126142495E07349220
chr62614269226142800E07349551
chr62614298226143055E07349841
chr62611886326118940E07425722
chr62611929226119516E07426151
chr62612842026128913E07435279
chr62612899426129044E07435853
chr62612977726129821E07436636
chr62612996726130171E07436826
chr62613017926130425E07437038
chr62613051426130656E07437373
chr62613094126131475E07437800
chr62613162426131707E07438483
chr62613171426131783E07438573
chr62613190126132235E07438760
chr62613224526132303E07439104
chr62613239026132718E07439249
chr62613283126132953E07439690
chr62613397626134065E07440835
chr62614034226140441E07447201
chr62614052126140673E07447380
chr62614089926141510E07447758
chr62614163726141810E07448496
chr62614182626142094E07448685
chr62614236126142495E07449220
chr62614269226142800E07449551
chr62614298226143055E07449841
chr62610502326105297E08111882
chr62612803326128083E08134892
chr62612825226128378E08135111
chr62612842026128913E08135279









Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr62604328026046649E067-46492
chr62605422326057549E067-35592
chr62608746126089220E067-3921
chr62610337026104998E06710229
chr62612234026127811E06729199
chr62604328026046649E068-46492
chr62605422326057549E068-35592
chr62608746126089220E068-3921
chr62610337026104998E06810229
chr62612234026127811E06829199
chr62604328026046649E069-46492
chr62605422326057549E069-35592
chr62608746126089220E069-3921
chr62610337026104998E06910229
chr62612234026127811E06929199
chr62604328026046649E070-46492
chr62605422326057549E070-35592
chr62610337026104998E07010229
chr62612234026127811E07029199
chr62604328026046649E071-46492
chr62605422326057549E071-35592
chr62608746126089220E071-3921
chr62610337026104998E07110229
chr62612234026127811E07129199
chr62604328026046649E072-46492
chr62605422326057549E072-35592
chr62608746126089220E072-3921
chr62610337026104998E07210229
chr62612234026127811E07229199
chr62604328026046649E073-46492
chr62605422326057549E073-35592
chr62608746126089220E073-3921
chr62610337026104998E07310229
chr62612234026127811E07329199
chr62604328026046649E074-46492
chr62605422326057549E074-35592
chr62608746126089220E074-3921
chr62610337026104998E07410229
chr62612234026127811E07429199
chr62605422326057549E081-35592
chr62610337026104998E08110229
chr62604328026046649E082-46492
chr62605422326057549E082-35592
chr62610337026104998E08210229
chr62612234026127811E08229199