| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101694855-101695250 | Common:1; Rare:90; Clinvar:2; Clinvar (benign):1 | ||||
| chr10:101818345-101818748 | Common:1; Rare:111 | ||||
| chr10:102502617-102502824 | Rare:65 | ||||
| chr10:102644971-102645163 | Rare:41 | ||||
| chr10:102714264-102714669 | Common:2; Rare:132 | ||||
| chr10:102776057-102776234 | Common:1; Rare:28 | ||||
| chr10:102854062-102854289 | Common:1; Rare:76 | ||||
| chr10:103396417-103396710 | Rare:105 | ||||
| chr10:103452261-103452436 | Rare:53 | ||||
| chr10:104268964-104269190 | Common:3; Rare:53 | ||||
| chr10:104338446-104338520 | Rare:19 | ||||
| chr10:110005899-110006098 | Common:4; Rare:57 | ||||
| chr10:110007668-110008100 | Common:1; Rare:126 | ||||
| chr10:110871616-110871956 | Rare:109 | ||||
| chr10:110919294-110919645 | Common:7; Rare:92; Clinvar:1 |