| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:38251300-38251700 | Common:7; Rare:75 | ||||
| chr15:39181071-39181471 | Common:2; Rare:93 | ||||
| chr15:39213492-39213803 | Common:2; Rare:65 | ||||
| chr15:39579352-39580093 | Common:8; Rare:211 | ||||
| chr15:39581953-39582730 | Common:4; Rare:269 | ||||
| chr15:39692570-39693100 | Common:1; Rare:87 | ||||
| chr15:39693166-39693283 | Rare:19 | ||||
| chr15:39704254-39704654 | Common:3; Rare:73 | ||||
| chr15:39704743-39705028 | Common:1; Rare:39 | ||||
| chr15:39771241-39771641 | Common:3; Rare:126 | ||||
| chr15:39778240-39778383 | Common:2; Rare:26 | ||||
| chr15:39783812-39784141 | Common:7; Rare:60 | ||||
| chr15:40003155-40003555 | Common:1; Rare:174; Clinvar (pathogenic):3 | ||||
| chr15:40081727-40081980 | Common:1; Rare:63 | ||||
| chr15:40092160-40092760 | Common:2; Rare:157 |