| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72229507-72229846 | Common:1; Rare:80 | ||||
| chr15:72230326-72230662 | Common:3; Rare:90 | ||||
| chr15:72231037-72231795 | Common:7; Rare:221 | ||||
| chr15:72232309-72232559 | Rare:45 | ||||
| chr15:72272465-72273038 | Common:3; Rare:152 | ||||
| chr15:72375623-72375799 | Rare:47; Clinvar:1; Clinvar (pathogenic):4 | ||||
| chr15:72375901-72376294 | Common:4; Rare:146; Clinvar:12; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473642-72473869 | Common:1; Rare:37 | ||||
| chr15:72473931-72474409 | Rare:142 | ||||
| chr15:72475080-72475345 | Common:1; Rare:77 | ||||
| chr15:72685889-72686446 | Common:3; Rare:161; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72783605-72784220 | Common:4; Rare:202 | ||||
| chr15:73051839-73051922 | Common:1; Rare:27 | ||||
| chr15:73051932-73051939 | Rare:2 | ||||
| chr15:73052208-73052381 | Common:2; Rare:43 |