| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42490993-42491214 | Common:1; Rare:68 | ||||
| chr15:42548698-42548874 | Common:2; Rare:92 | ||||
| chr15:43330555-43330767 | Common:1; Rare:75 | ||||
| chr15:43371043-43371108 | Rare:13 | ||||
| chr15:43510610-43510998 | Rare:133 | ||||
| chr15:43746287-43746438 | Common:1; Rare:57 | ||||
| chr15:43777116-43777409 | Rare:65 | ||||
| chr15:43824573-43824811 | Common:2; Rare:69 | ||||
| chr15:44288417-44288737 | Common:35; Rare:202 | ||||
| chr15:44536863-44537218 | Common:2; Rare:128 | ||||
| chr15:44711378-44711611 | Rare:78; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45378532-45378717 | Common:3; Rare:45; Clinvar (benign):1 | ||||
| chr15:45587319-45587446 | Rare:42; Clinvar:4 | ||||
| chr15:47718382-47718595 | Common:1; Rare:53 | ||||
| chr15:48645710-48645989 | Common:2; Rare:90; Clinvar (benign):1 |