Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:114581532-114581811 | Common:1; Rare:126 | ||||
chr1:114669986-114670259 | Common:1; Rare:85 | ||||
chr1:114716713-114716891 | Common:1; Rare:81; Clinvar:5; Clinvar (benign):1 | ||||
chr1:116373073-116373521 | Common:3; Rare:145 | ||||
chr1:116387216-116387320 | Rare:22 | ||||
chr1:116388428-116388770 | Common:2; Rare:63 | ||||
chr1:116399219-116399541 | Rare:54 | ||||
chr1:116400760-116400877 | Common:1; Rare:29; Clinvar (pathogenic):1 | ||||
chr1:116666896-116667172 | Rare:54 | ||||
chr1:116909707-116910125 | Common:1; Rare:119 | ||||
chr1:117060010-117060374 | Common:7; Rare:105 | ||||
chr1:117929555-117929807 | Common:4; Rare:76 | ||||
chr1:119140629-119140677 | Rare:25 | ||||
chr1:121184828-121185360 | Common:1; Rare:129 | ||||
chr1:121185495-121185659 | Rare:10 |