rs10649162

Homo sapiens
dupAG
None
Check p-value
Indel (Insertion and Deletion)
AG==0150 (753/5008,1000G)
AG==0211 (815/3854,ALSPAC)
AG==0205 (760/3708,TWINSUK)
chr6:153299421-153299422 (GRCh38.p7) (6q25.2)
AD
GWASCatalog
1   publication(s)
See rs on genome
5 Enhancers around
0 Promoter around

Genomic Coordinates

Sequence Name Change(s)
GRCh38.p7 chr 6NC_000006.12:g.153299421_153299422dup
GRCh37.p13 chr 6NC_000006.11:g.153620556_153620557dup

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 )
chr6153625642153625682E0705086
chr6153627745153627809E0707189
chr6153628942153628996E0708386
chr6153633705153634161E07013149
chr6153634202153634263E07013646

Mpgyi