| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40405632-40405839 | Common:2; Rare:65; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr15:40439558-40439789 | Rare:38 | ||||
| chr15:40569176-40569360 | Common:3; Rare:44 | ||||
| chr15:40695076-40695236 | Common:2; Rare:49 | ||||
| chr15:40755212-40755424 | Common:2; Rare:71 | ||||
| chr15:40763928-40764125 | Rare:50 | ||||
| chr15:40807436-40807805 | Common:5; Rare:122 | ||||
| chr15:40844307-40844692 | Rare:135 | ||||
| chr15:40853572-40853871 | Common:2; Rare:99 | ||||
| chr15:40854478-40854683 | Common:2; Rare:64 | ||||
| chr15:40894178-40894473 | Rare:85 | ||||
| chr15:40953160-40953488 | Common:2; Rare:88 | ||||
| chr15:41230754-41230831 | Rare:17 | ||||
| chr15:41231039-41231433 | Rare:120 | ||||
| chr15:41402458-41402558 | Common:2; Rare:30 |