| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:101032565-101032863 | Common:1; Rare:82 | ||||
| chr10:101042671-101042866 | Common:2; Rare:33 | ||||
| chr10:101042870-101043299 | Rare:90 | ||||
| chr10:101043540-101043609 | Rare:15 | ||||
| chr10:101060623-101061330 | Common:4; Rare:191 | ||||
| chr10:101067620-101067776 | Common:2; Rare:29 | ||||
| chr10:101067845-101068020 | Common:1; Rare:43 | ||||
| chr10:101112999-101113493 | Common:5; Rare:100 | ||||
| chr10:101139763-101139892 | Rare:29 | ||||
| chr10:101530146-101530461 | Rare:46 | ||||
| chr10:101569781-101569981 | Rare:45 | ||||
| chr10:101630338-101630610 | Common:1; Rare:46 | ||||
| chr10:101693785-101693894 | Common:1; Rare:19 | ||||
| chr10:101694015-101694140 | Rare:28 | ||||
| chr10:101694245-101694627 | Common:1; Rare:115; Clinvar:3; Clinvar (benign):2 |