| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:34794678-34794949 | Rare:68; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:40326040-40326112 | Rare:16 | ||||
| chr15:51094651-51094988 | Common:8; Rare:88 | ||||
| chr15:57602564-57602724 | Common:1; Rare:43 | ||||
| chr15:58549913-58550050 | Rare:25 | ||||
| chr15:64774351-64774410 | Rare:12 | ||||
| chr15:82750445-82750591 | Common:2; Rare:37 | ||||
| chr15:84570768-84570835 | Rare:17 | ||||
| chr15:84570853-84571070 | Common:4; Rare:60 | ||||
| chr15:84631314-84631477 | Common:3; Rare:45 | ||||
| chr15:85494412-85494650 | Common:1; Rare:49 | ||||
| chr15:89104367-89104558 | Common:1; Rare:41 | ||||
| chr15:95326873-95327055 | Common:1; Rare:63 | ||||
| chr15:96327323-96327420 | Common:3; Rare:16 | ||||
| chr15:98840173-98840473 | Common:2; Rare:63 |