| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:14878606-14878901 | Common:2; Rare:94 | ||||
| chr10:14954030-14954156 | Rare:38 | ||||
| chr10:15097319-15097401 | Common:1; Rare:38 | ||||
| chr10:17229124-17229381 | Common:1; Rare:56 | ||||
| chr10:17643871-17644276 | Common:2; Rare:122 | ||||
| chr10:18651570-18651773 | Common:1; Rare:85 | ||||
| chr10:21533943-21534253 | Common:1; Rare:115 | ||||
| chr10:22321362-22321608 | Rare:87 | ||||
| chr10:24208812-24209184 | Rare:105 | ||||
| chr10:27154315-27154476 | Rare:42 | ||||
| chr10:27155212-27155376 | Common:4; Rare:55; Clinvar:2; Clinvar (benign):4 | ||||
| chr10:27240575-27240888 | Common:2; Rare:83 | ||||
| chr10:28532480-28532862 | Common:5; Rare:154 | ||||
| chr10:28532992-28533205 | Rare:87 | ||||
| chr10:29634278-29635071 | Common:2; Rare:147 |