| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:49620762-49621099 | Common:6; Rare:128 | ||||
| chr15:50182326-50182454 | Rare:36 | ||||
| chr15:50354885-50355004 | Rare:17 | ||||
| chr15:50355074-50355501 | Common:3; Rare:168 | ||||
| chr15:50424156-50424530 | Common:2; Rare:132 | ||||
| chr15:50686717-50686914 | Common:4; Rare:82 | ||||
| chr15:50765529-50765756 | Common:2; Rare:79 | ||||
| chr15:50908574-50908765 | Common:2; Rare:79; Clinvar (benign):2 | ||||
| chr15:51341733-51341895 | Common:1; Rare:50; Clinvar (pathogenic):1 | ||||
| chr15:51681411-51681538 | Common:1; Rare:22 | ||||
| chr15:51751488-51751694 | Common:1; Rare:55 | ||||
| chr15:51971719-51971831 | Rare:56 | ||||
| chr15:52019104-52019275 | Common:1; Rare:86 | ||||
| chr15:52179836-52180057 | Common:1; Rare:80 | ||||
| chr15:52678733-52678831 | Common:1; Rare:27 |