| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:7787926-7788260 | Common:1; Rare:140 | ||||
| chr10:12195809-12195981 | Rare:46 | ||||
| chr10:13099818-13100217 | Common:4; Rare:96; Clinvar:3; Clinvar (benign):5 | ||||
| chr10:13300044-13300189 | Rare:52; Clinvar:1 | ||||
| chr10:14838058-14838321 | Common:2; Rare:73 | ||||
| chr10:14838677-14838934 | Common:1; Rare:73 | ||||
| chr10:14878634-14878886 | Common:2; Rare:76 | ||||
| chr10:17230016-17230132 | Common:2; Rare:38 | ||||
| chr10:17233591-17233923 | Common:2; Rare:107; Clinvar (benign):1 | ||||
| chr10:17453932-17454196 | Common:1; Rare:68 | ||||
| chr10:17454305-17454652 | Common:1; Rare:93 | ||||
| chr10:17454653-17454763 | Common:1; Rare:24 | ||||
| chr10:17643850-17644336 | Common:3; Rare:159 | ||||
| chr10:18659256-18659511 | Common:2; Rare:90 | ||||
| chr10:27154184-27154495 | Rare:88 |