| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72222566-72222748 | Rare:35 | ||||
| chr15:72228557-72228964 | Common:2; Rare:88 | ||||
| chr15:72229004-72229104 | Common:1; Rare:18 | ||||
| chr15:72229188-72229346 | Rare:28 | ||||
| chr15:72229480-72229572 | Common:1; Rare:23 | ||||
| chr15:72230098-72230655 | Common:3; Rare:148 | ||||
| chr15:72230924-72231565 | Common:6; Rare:214 | ||||
| chr15:72231606-72231887 | Common:2; Rare:54 | ||||
| chr15:72232235-72232375 | Rare:26 | ||||
| chr15:72271925-72272150 | Common:1; Rare:61 | ||||
| chr15:72272320-72273048 | Common:3; Rare:182 | ||||
| chr15:72375564-72375794 | Common:1; Rare:55; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr15:72375823-72376031 | Common:1; Rare:85; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
| chr15:72376035-72376300 | Common:2; Rare:85; Clinvar:5 | ||||
| chr15:72376418-72376528 | Rare:28 |