Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113812264-113812587 | Common:2; Rare:127 | ||||
chr1:113905026-113905385 | Common:5; Rare:100 | ||||
chr1:115089446-115089622 | Common:3; Rare:71 | ||||
chr1:115641783-115642027 | Common:3; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr1:116399212-116399543 | Rare:55 | ||||
chr1:117605771-117606048 | Rare:78 | ||||
chr1:117929552-117929839 | Common:4; Rare:88 | ||||
chr1:119140595-119140768 | Common:1; Rare:62; Clinvar (pathogenic):1 | ||||
chr1:119648141-119648364 | Common:3; Rare:78 | ||||
chr1:120176343-120176681 | Common:1; Rare:63 | ||||
chr1:145823869-145824251 | Rare:132 | ||||
chr1:145858968-145859175 | Rare:60 | ||||
chr1:145918686-145919013 | Common:2; Rare:70 | ||||
chr1:145927364-145927644 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:145958000-145958202 | Rare:47 |