| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:83284593-83284906 | Rare:108 | ||||
| chr15:84600856-84601070 | Rare:60 | ||||
| chr15:84716389-84716556 | Rare:40 | ||||
| chr15:85380375-85380693 | Common:1; Rare:104 | ||||
| chr15:88467336-88467951 | Common:7; Rare:214 | ||||
| chr15:89243725-89244042 | Common:2; Rare:97; Clinvar:3 | ||||
| chr15:89334791-89335069 | Common:3; Rare:104 | ||||
| chr15:90102443-90102585 | Rare:50 | ||||
| chr15:90233881-90234292 | Common:6; Rare:114 | ||||
| chr15:90265554-90265876 | Common:1; Rare:136 | ||||
| chr15:90351947-90352323 | Common:5; Rare:87 | ||||
| chr15:90387961-90388382 | Common:5; Rare:168 | ||||
| chr15:90717134-90717395 | Rare:63; Clinvar:2 | ||||
| chr15:90994443-90994729 | Common:1; Rare:103 | ||||
| chr15:91022531-91022624 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):1 |