Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:101694896-101695216 | Rare:78; Clinvar:2 | ||||
chr10:101817983-101818762 | Common:1; Rare:229 | ||||
chr10:102033087-102033328 | Rare:63 | ||||
chr10:102056089-102056326 | Common:1; Rare:58 | ||||
chr10:102394348-102394570 | Rare:60 | ||||
chr10:102395574-102395721 | Common:1; Rare:41 | ||||
chr10:102420818-102421215 | Rare:127 | ||||
chr10:102421538-102421617 | Common:1; Rare:19 | ||||
chr10:102432556-102432712 | Common:1; Rare:38 | ||||
chr10:102644988-102645163 | Rare:38 | ||||
chr10:102714271-102714669 | Common:2; Rare:129 | ||||
chr10:102917965-102918361 | Common:1; Rare:129 | ||||
chr10:103193248-103193321 | Common:4; Rare:23; Clinvar (benign):1 | ||||
chr10:103396407-103396709 | Rare:108 | ||||
chr10:103452275-103452446 | Rare:49 |