Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:115089462-115089606 | Common:2; Rare:53 | ||||
chr1:115641803-115642063 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr1:115976228-115976571 | Rare:105 | ||||
chr1:116123943-116124155 | Common:2; Rare:62 | ||||
chr1:116373093-116373520 | Common:3; Rare:141 | ||||
chr1:116570961-116571135 | Common:1; Rare:54 | ||||
chr1:116754345-116754497 | Rare:42 | ||||
chr1:117060180-117060360 | Common:2; Rare:51 | ||||
chr1:117367323-117367531 | Common:5; Rare:69 | ||||
chr1:117929555-117929879 | Common:4; Rare:98 | ||||
chr1:119140597-119140691 | Rare:43; Clinvar (pathogenic):1 | ||||
chr1:145607969-145608069 | Rare:38 | ||||
chr1:145823895-145824336 | Rare:148 | ||||
chr1:145858986-145859154 | Rare:48 | ||||
chr1:145885814-145886183 | Common:1; Rare:78 |