| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:13099717-13099946 | Common:1; Rare:54 | ||||
| chr10:13099952-13100295 | Common:4; Rare:79; Clinvar:3; Clinvar (benign):6 | ||||
| chr10:13707141-13707283 | Common:2; Rare:26 | ||||
| chr10:13707548-13707626 | Rare:16 | ||||
| chr10:14532679-14532895 | Common:2; Rare:46 | ||||
| chr10:14572044-14572313 | Common:3; Rare:46 | ||||
| chr10:14837968-14838395 | Common:2; Rare:128 | ||||
| chr10:14878637-14878891 | Common:2; Rare:76 | ||||
| chr10:14953994-14954202 | Rare:76 | ||||
| chr10:15097319-15097401 | Common:1; Rare:38 | ||||
| chr10:15860442-15860540 | Rare:26 | ||||
| chr10:17229121-17229333 | Common:1; Rare:43 | ||||
| chr10:17643871-17644297 | Common:2; Rare:131 | ||||
| chr10:18651514-18651710 | Common:1; Rare:75 | ||||
| chr10:18659221-18659491 | Common:2; Rare:95 |