Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:116570945-116571107 | Rare:47 | ||||
chr1:116909811-116910207 | Common:1; Rare:124 | ||||
chr1:117060037-117060359 | Common:7; Rare:86 | ||||
chr1:117929552-117929811 | Common:4; Rare:79 | ||||
chr1:119140634-119140771 | Common:1; Rare:43 | ||||
chr1:119648136-119648350 | Common:3; Rare:77 | ||||
chr1:120176343-120176647 | Common:1; Rare:59 | ||||
chr1:121087318-121087386 | Rare:24 | ||||
chr1:143905978-143906253 | Rare:60 | ||||
chr1:144461570-144461672 | Common:4; Rare:43 | ||||
chr1:145823869-145824286 | Rare:145 | ||||
chr1:145858965-145859085 | Rare:39 | ||||
chr1:145859759-145859824 | Rare:32 | ||||
chr1:145918680-145919043 | Common:2; Rare:82 | ||||
chr1:145927379-145927669 | Common:1; Rare:80; Clinvar (pathogenic):1 |