| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70854101-70854274 | Rare:57 | ||||
| chr15:70892641-70892851 | Rare:43 | ||||
| chr15:72117950-72118434 | Common:5; Rare:168 | ||||
| chr15:72163442-72163751 | Common:1; Rare:90 | ||||
| chr15:72197753-72197982 | Common:3; Rare:91 | ||||
| chr15:72230213-72230498 | Rare:74 | ||||
| chr15:72231117-72231534 | Common:3; Rare:136 | ||||
| chr15:72231589-72231703 | Common:1; Rare:24 | ||||
| chr15:72272455-72272836 | Common:1; Rare:106 | ||||
| chr15:72375852-72376129 | Common:2; Rare:105; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr15:72474206-72474652 | Rare:153 | ||||
| chr15:72475152-72475293 | Common:1; Rare:39 | ||||
| chr15:72686111-72686220 | Common:2; Rare:41; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783481-72783597 | Rare:35 | ||||
| chr15:72783692-72783776 | Common:1; Rare:35 |