| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41416985-41417202 | Common:3; Rare:96 | ||||
| chr15:42273029-42273272 | Common:1; Rare:100 | ||||
| chr15:42273397-42273523 | Rare:49 | ||||
| chr15:42491002-42491206 | Common:1; Rare:63 | ||||
| chr15:42548725-42548870 | Common:2; Rare:80 | ||||
| chr15:43330573-43330694 | Rare:42 | ||||
| chr15:43510688-43510954 | Rare:85 | ||||
| chr15:43746282-43746423 | Common:1; Rare:50 | ||||
| chr15:43777116-43777386 | Rare:64 | ||||
| chr15:44536663-44537209 | Common:1; Rare:167 | ||||
| chr15:44711367-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45129845-45130004 | Rare:34 | ||||
| chr15:45587117-45587254 | Rare:24 | ||||
| chr15:45587321-45587450 | Rare:41; Clinvar:4 | ||||
| chr15:45587706-45587760 | Rare:15 |