| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:17643871-17644324 | Common:2; Rare:144 | ||||
| chr10:17809086-17809392 | Rare:39 | ||||
| chr10:18140429-18140889 | Common:4; Rare:154; Clinvar:5; Clinvar (benign):9 | ||||
| chr10:18141147-18141172 | Rare:7 | ||||
| chr10:18651543-18651748 | Common:1; Rare:86 | ||||
| chr10:18659230-18659680 | Common:2; Rare:153 | ||||
| chr10:21524503-21524653 | Rare:31 | ||||
| chr10:21526378-21526568 | Common:1; Rare:61 | ||||
| chr10:21533636-21533756 | Rare:23 | ||||
| chr10:21533966-21534337 | Common:3; Rare:151 | ||||
| chr10:22316270-22316546 | Common:1; Rare:119 | ||||
| chr10:22321304-22321600 | Rare:103 | ||||
| chr10:24208748-24209200 | Common:1; Rare:129 | ||||
| chr10:24238928-24239229 | Common:1; Rare:32 | ||||
| chr10:24466304-24466561 | Rare:39 |