| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:71096805-71096977 | Rare:27 | ||||
| chr15:72118010-72118468 | Common:3; Rare:157 | ||||
| chr15:72228594-72228686 | Common:1; Rare:35 | ||||
| chr15:72230407-72230654 | Common:3; Rare:74 | ||||
| chr15:72230941-72231505 | Common:5; Rare:180 | ||||
| chr15:72231543-72231653 | Common:2; Rare:27 | ||||
| chr15:72231692-72231705 | Rare:1 | ||||
| chr15:72375848-72376103 | Common:2; Rare:100; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):6 | ||||
| chr15:72474219-72474351 | Rare:46 | ||||
| chr15:72475290-72475576 | Common:3; Rare:63 | ||||
| chr15:73632386-73632495 | Rare:28 | ||||
| chr15:73633208-73633587 | Common:2; Rare:147 | ||||
| chr15:73926322-73926885 | Common:1; Rare:130 | ||||
| chr15:73994578-73994828 | Common:1; Rare:54 | ||||
| chr15:74202419-74202890 | Common:2; Rare:97; Clinvar:2 |