| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44427050-44427224 | Common:1; Rare:42 | ||||
| chr15:44536863-44537236 | Common:3; Rare:138 | ||||
| chr15:44711341-44711614 | Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45587072-45587530 | Common:2; Rare:118; Clinvar:7; Clinvar (benign):2 | ||||
| chr15:48645653-48646024 | Common:2; Rare:114; Clinvar (benign):1 | ||||
| chr15:48878007-48878192 | Rare:75 | ||||
| chr15:49155535-49155838 | Common:2; Rare:100 | ||||
| chr15:49620774-49621122 | Common:6; Rare:134 | ||||
| chr15:50355083-50355504 | Common:3; Rare:167 | ||||
| chr15:50424156-50424497 | Common:2; Rare:121 | ||||
| chr15:50686720-50686742 | Common:1; Rare:6 | ||||
| chr15:51971743-51971841 | Rare:44 | ||||
| chr15:52678624-52678897 | Common:1; Rare:82 | ||||
| chr15:55318932-55318962 | Rare:10 | ||||
| chr15:55319062-55319247 | Common:3; Rare:47 |