| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105487743-105487994 | Rare:146 | ||||
| chr14:105490121-105490232 | Common:3; Rare:42 | ||||
| chr14:105490993-105491386 | Common:2; Rare:233 | ||||
| chr15:22786463-22786816 | Rare:195; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr15:22838430-22838754 | Common:4; Rare:224 | ||||
| chr15:22980291-22980511 | Rare:151 | ||||
| chr15:23039536-23039753 | Common:2; Rare:170 | ||||
| chr15:23565533-23565730 | Common:1; Rare:99 | ||||
| chr15:25437990-25438470 | Common:2; Rare:160 | ||||
| chr15:25438490-25439261 | Common:6; Rare:384 | ||||
| chr15:29269754-29269925 | Common:4; Rare:144 | ||||
| chr15:29822026-29822226 | Rare:110 | ||||
| chr15:29822314-29822649 | Common:4; Rare:217 | ||||
| chr15:30903686-30903954 | Common:3; Rare:116 | ||||
| chr15:30991521-30991800 | Common:8; Rare:188 |