Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:117121663-117122013 | Common:1; Rare:112 | ||||
chr1:117366641-117367117 | Common:1; Rare:134 | ||||
chr1:117367204-117367799 | Common:7; Rare:172 | ||||
chr1:117605768-117606110 | Rare:104 | ||||
chr1:117928877-117929114 | Rare:50 | ||||
chr1:117929509-117930013 | Common:5; Rare:139 | ||||
chr1:118989502-118989588 | Common:2; Rare:24 | ||||
chr1:119140301-119140490 | Common:2; Rare:53 | ||||
chr1:119140537-119140843 | Common:1; Rare:102; Clinvar (pathogenic):1 | ||||
chr1:119141128-119141160 | Rare:7 | ||||
chr1:119647673-119647915 | Rare:39 | ||||
chr1:119648066-119648587 | Common:5; Rare:156 | ||||
chr1:119711786-119711995 | Common:2; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
chr1:120175848-120176198 | Common:1; Rare:43 | ||||
chr1:120176254-120176303 | Rare:8 |