Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:110919129-110919309 | Common:1; Rare:46 | ||||
chr10:110919330-110919654 | Common:7; Rare:90; Clinvar:1; Clinvar (benign):1 | ||||
chr10:112446729-112447334 | Common:3; Rare:148 | ||||
chr10:112950968-112951256 | Common:2; Rare:73 | ||||
chr10:113678961-113679299 | Common:3; Rare:62 | ||||
chr10:113854177-113855011 | Common:2; Rare:190 | ||||
chr10:113855013-113855042 | Rare:14 | ||||
chr10:114526665-114526725 | Rare:13 | ||||
chr10:114821647-114821990 | Common:1; Rare:111 | ||||
chr10:116273572-116273925 | Common:17; Rare:73 | ||||
chr10:118046114-118046351 | Common:1; Rare:72 | ||||
chr10:118046454-118046460 | |||||
chr10:118046575-118047021 | Common:4; Rare:140 | ||||
chr10:118754906-118755339 | Common:2; Rare:148 | ||||
chr10:119080772-119080889 | Rare:53 |