| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13099966-13100201 | Common:2; Rare:62; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:13348017-13348335 | Rare:102 | ||||
| chr10:14838023-14838361 | Common:2; Rare:89 | ||||
| chr10:14878637-14878891 | Common:2; Rare:76 | ||||
| chr10:14954062-14954153 | Rare:18 | ||||
| chr10:15097328-15097401 | Common:1; Rare:33 | ||||
| chr10:15860469-15860592 | Rare:34 | ||||
| chr10:16817373-16817734 | Common:3; Rare:129 | ||||
| chr10:17228964-17229291 | Common:3; Rare:66 | ||||
| chr10:17643860-17644291 | Common:2; Rare:131 | ||||
| chr10:18651553-18651778 | Common:1; Rare:92 | ||||
| chr10:19816143-19816432 | Common:5; Rare:67 | ||||
| chr10:21524545-21524740 | Rare:30 | ||||
| chr10:21526404-21526581 | Common:1; Rare:57 | ||||
| chr10:22316210-22316438 | Common:2; Rare:102 |