| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14008420-14008496 | Rare:20 | ||||
| chr10:14008498-14008716 | Common:2; Rare:42 | ||||
| chr10:14604241-14604570 | Common:5; Rare:142 | ||||
| chr10:14837994-14838415 | Common:4; Rare:119 | ||||
| chr10:14878597-14878907 | Common:2; Rare:100 | ||||
| chr10:14953937-14954202 | Rare:92; Clinvar (benign):1 | ||||
| chr10:14954322-14954363 | Rare:4 | ||||
| chr10:15097301-15097401 | Common:1; Rare:50 | ||||
| chr10:15719568-15719791 | Common:4; Rare:69 | ||||
| chr10:15719868-15719998 | Common:1; Rare:46 | ||||
| chr10:15860260-15860583 | Common:2; Rare:89 | ||||
| chr10:16817313-16817844 | Common:5; Rare:178 | ||||
| chr10:17228542-17228675 | Common:1; Rare:36 | ||||
| chr10:17228929-17229247 | Common:3; Rare:66 | ||||
| chr10:17230167-17230710 | Common:2; Rare:157; Clinvar:1 |