| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231107-72231542 | Common:3; Rare:142 | ||||
| chr15:72272491-72272590 | Rare:29 | ||||
| chr15:72375938-72376166 | Common:3; Rare:92; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72474138-72474281 | Rare:50 | ||||
| chr15:72686147-72686441 | Common:2; Rare:97; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72783516-72783876 | Common:2; Rare:150 | ||||
| chr15:73633202-73633595 | Common:2; Rare:155 | ||||
| chr15:73684071-73684449 | Rare:105 | ||||
| chr15:73926313-73926498 | Rare:52 | ||||
| chr15:73992268-73992441 | Common:1; Rare:49 | ||||
| chr15:73994587-73994730 | Rare:27 | ||||
| chr15:74100167-74100319 | Rare:21 | ||||
| chr15:74130067-74130403 | Rare:75 | ||||
| chr15:74173787-74173876 | Common:2; Rare:20 | ||||
| chr15:74174412-74174576 | Common:1; Rare:27 |