| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:15096968-15097277 | Common:5; Rare:115 | ||||
| chr10:15097298-15097401 | Common:1; Rare:53 | ||||
| chr10:15860455-15860583 | Rare:36 | ||||
| chr10:16817313-16817744 | Common:5; Rare:153 | ||||
| chr10:17228463-17228675 | Common:1; Rare:57 | ||||
| chr10:17228930-17229026 | Common:1; Rare:26 | ||||
| chr10:17230485-17230710 | Common:1; Rare:88; Clinvar:1 | ||||
| chr10:17643871-17644295 | Common:2; Rare:129 | ||||
| chr10:18651564-18651748 | Common:1; Rare:80 | ||||
| chr10:18659230-18659573 | Common:2; Rare:111 | ||||
| chr10:19815696-19815867 | Rare:50 | ||||
| chr10:19816183-19816634 | Common:6; Rare:107 | ||||
| chr10:21173754-21174335 | Common:4; Rare:165; Clinvar (benign):1 | ||||
| chr10:21526398-21526625 | Common:1; Rare:77 | ||||
| chr10:21533955-21534507 | Common:3; Rare:208 |