| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101818324-101818778 | Common:1; Rare:125 | ||||
| chr10:102056088-102056348 | Common:1; Rare:60 | ||||
| chr10:102065264-102065487 | Common:1; Rare:83 | ||||
| chr10:102114498-102114561 | Rare:19 | ||||
| chr10:102120296-102120570 | Common:2; Rare:93 | ||||
| chr10:102152307-102152598 | Common:1; Rare:128 | ||||
| chr10:102394336-102394500 | Rare:45 | ||||
| chr10:102395553-102395772 | Common:1; Rare:56 | ||||
| chr10:102400761-102401014 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:102420718-102421247 | Rare:161 | ||||
| chr10:102432530-102432791 | Common:1; Rare:79 | ||||
| chr10:102502624-102502904 | Common:1; Rare:85 | ||||
| chr10:102714267-102714665 | Common:2; Rare:131 | ||||
| chr10:102776078-102776251 | Common:1; Rare:29 | ||||
| chr10:103367845-103367989 | Common:2; Rare:23 |