| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:102714275-102714636 | Common:2; Rare:121 | ||||
| chr10:102854251-102854280 | Rare:13 | ||||
| chr10:102854448-102854651 | Common:1; Rare:51 | ||||
| chr10:103181327-103181492 | Common:3; Rare:36 | ||||
| chr10:103350939-103351186 | Common:2; Rare:102 | ||||
| chr10:103367815-103367982 | Common:3; Rare:30 | ||||
| chr10:103396386-103396715 | Rare:118 | ||||
| chr10:103918158-103918540 | Common:3; Rare:100 | ||||
| chr10:104121878-104122171 | Common:2; Rare:93 | ||||
| chr10:104254838-104254931 | Rare:27 | ||||
| chr10:104268885-104269253 | Common:4; Rare:94 | ||||
| chr10:109923429-109923663 | Common:2; Rare:89 | ||||
| chr10:110007684-110008013 | Rare:100 | ||||
| chr10:110567381-110567781 | Common:2; Rare:115; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110871728-110871960 | Rare:72 |