rs4747764

Homo sapiens
G>A
None
Check p-value
SNV (Single Nucleotide Variation)
A=0238 (7151/29944,GnomAD)
A=0205 (5991/29118,TOPMED)
A=0259 (1297/5008,1000G)
A=0228 (877/3854,ALSPAC)
A=0235 (871/3708,TWINSUK)
chr10:32068628 (GRCh38.p7) (10p11.22)
AD
GWASdb2
1   publication(s)
See rs on genome
91 Enhancers around
30 Promoters around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 10NC_000010.11:g.32068628G>A
GRCh37.p13 chr 10NC_000010.10:g.32357556G>A

Population Frequency

Study Population Group Sample # Ref Allele Alt Allele
1000GenomesAfricanSub1322G=0.840A=0.160
1000GenomesAmericanSub694G=0.770A=0.230
1000GenomesEast AsianSub1008G=0.530A=0.470
1000GenomesEuropeSub1006G=0.778A=0.222
1000GenomesGlobalStudy-wide5008G=0.741A=0.259
1000GenomesSouth AsianSub978G=0.770A=0.230
The Avon Longitudinal Study of Parents and ChildrenPARENT AND CHILD COHORTStudy-wide3854G=0.772A=0.228
The Genome Aggregation DatabaseAfricanSub8722G=0.834A=0.166
The Genome Aggregation DatabaseAmericanSub838G=0.760A=0.240
The Genome Aggregation DatabaseEast AsianSub1612G=0.525A=0.475
The Genome Aggregation DatabaseEuropeSub18470G=0.747A=0.253
The Genome Aggregation DatabaseGlobalStudy-wide29944G=0.761A=0.238
The Genome Aggregation DatabaseOtherSub302G=0.770A=0.230
Trans-Omics for Precision MedicineGlobalStudy-wide29118G=0.794A=0.205
UK 10K study - TwinsTWIN COHORTStudy-wide3708G=0.765A=0.235
PMID Title Author Journal
20201924Genome-wide association study of alcohol dependence implicates a region on chromosome 11.Edenberg HJAlcohol Clin Exp Res

P-Value

SNP ID p-value Traits Study
rs47477640.00081alcohol dependence20201924

eQTL of rs4747764 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 rs4747764 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 )
chr103233130732331357E067-26199
chr103233147432331530E067-26026
chr103233791532338569E067-18987
chr103233877532338849E067-18707
chr103233887132339138E067-18418
chr103233918432339465E067-18091
chr103233947332339647E067-17909
chr103233970232339742E067-17814
chr103234123432341451E067-16105
chr103234148532341628E067-15928
chr103234630832346550E067-11006
chr103233045432330506E068-27050
chr103233060332330705E068-26851
chr103233079932330849E068-26707
chr103233791532338569E068-18987
chr103233877532338849E068-18707
chr103233887132339138E068-18418
chr103233918432339465E068-18091
chr103233947332339647E068-17909
chr103233970232339742E068-17814
chr103233992832340032E068-17524
chr103234123432341451E068-16105
chr103233877532338849E069-18707
chr103233887132339138E069-18418
chr103233918432339465E069-18091
chr103233947332339647E069-17909
chr103233970232339742E069-17814
chr103233992832340032E069-17524
chr103234039032340440E069-17116
chr103234058732340660E069-16896
chr103234123432341451E069-16105
chr103234148532341628E069-15928
chr103234166932341730E069-15826
chr103234177032341820E069-15736
chr103234190432341954E069-15602
chr103233045432330506E070-27050
chr103233060332330705E070-26851
chr103233079932330849E070-26707
chr103233791532338569E070-18987
chr103233877532338849E070-18707
chr103233887132339138E070-18418
chr103233918432339465E070-18091
chr103233947332339647E070-17909
chr103233970232339742E070-17814
chr103234058732340660E070-16896
chr103234123432341451E070-16105
chr103234148532341628E070-15928
chr103234166932341730E070-15826
chr103234177032341820E070-15736
chr103234190432341954E070-15602
chr103233147432331530E071-26026
chr103233170132331963E071-25593
chr103233791532338569E071-18987
chr103233877532338849E071-18707
chr103233887132339138E071-18418
chr103233918432339465E071-18091
chr103233947332339647E071-17909
chr103233970232339742E071-17814
chr103233992832340032E071-17524
chr103234039032340440E071-17116
chr103234058732340660E071-16896
chr103234148532341628E071-15928
chr103234166932341730E071-15826
chr103234177032341820E071-15736
chr103234190432341954E071-15602
chr103232933132329390E072-28166
chr103233791532338569E072-18987
chr103233887132339138E072-18418
chr103233918432339465E072-18091
chr103233947332339647E072-17909
chr103234123432341451E072-16105
chr103233918432339465E073-18091
chr103234123432341451E073-16105
chr103234630832346550E073-11006
chr103233147432331530E074-26026
chr103233170132331963E074-25593
chr103233887132339138E074-18418
chr103233918432339465E074-18091
chr103233992832340032E074-17524
chr103234039032340440E074-17116
chr103234058732340660E074-16896
chr103234123432341451E074-16105
chr103234123432341451E081-16105
chr103234148532341628E081-15928
chr103234166932341730E081-15826
chr103234177032341820E081-15736
chr103234190432341954E081-15602
chr103233918432339465E082-18091
chr103233947332339647E082-17909
chr103234177032341820E082-15736
chr103234190432341954E082-15602










Promoter Annotation (GRCh37.p13)

Chromosome Start End Region Distance(-/+:Up/Downstream)
chr103234267432343924E067-13632
chr103234400932344126E067-13430
chr103234413732345903E067-11653
chr103234267432343924E068-13632
chr103234400932344126E068-13430
chr103234413732345903E068-11653
chr103234267432343924E069-13632
chr103234400932344126E069-13430
chr103234413732345903E069-11653
chr103234267432343924E070-13632
chr103234400932344126E070-13430
chr103234413732345903E070-11653
chr103234267432343924E071-13632
chr103234400932344126E071-13430
chr103234413732345903E071-11653
chr103234267432343924E072-13632
chr103234400932344126E072-13430
chr103234413732345903E072-11653
chr103234267432343924E073-13632
chr103234400932344126E073-13430
chr103234413732345903E073-11653
chr103234267432343924E074-13632
chr103234400932344126E074-13430
chr103234413732345903E074-11653
chr103234267432343924E081-13632
chr103234400932344126E081-13430
chr103234413732345903E081-11653
chr103234267432343924E082-13632
chr103234400932344126E082-13430
chr103234413732345903E082-11653