Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:102502648-102502894 | Common:1; Rare:81 | ||||
chr10:102644982-102645147 | Rare:36 | ||||
chr10:102714271-102714659 | Common:2; Rare:127 | ||||
chr10:103193250-103193548 | Common:4; Rare:81 | ||||
chr10:103396419-103396710 | Rare:104 | ||||
chr10:110006011-110006084 | Common:2; Rare:20 | ||||
chr10:110007776-110008043 | Rare:66 | ||||
chr10:110008610-110008922 | Common:6; Rare:84 | ||||
chr10:110227230-110227357 | Common:2; Rare:12 | ||||
chr10:110871622-110871970 | Rare:115 | ||||
chr10:110872336-110872649 | Common:1; Rare:110 | ||||
chr10:110919326-110919620 | Common:7; Rare:78 | ||||
chr10:111076734-111077039 | Common:2; Rare:81; Clinvar (benign):1 | ||||
chr10:112215351-112215641 | Rare:46 | ||||
chr10:112446877-112447283 | Common:3; Rare:100 |