| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43330602-43330738 | Common:1; Rare:44 | ||||
| chr15:43371017-43371160 | Common:1; Rare:33 | ||||
| chr15:43510688-43510954 | Rare:85 | ||||
| chr15:43517497-43517653 | Common:2; Rare:38 | ||||
| chr15:43746287-43746461 | Common:1; Rare:67 | ||||
| chr15:43824585-43824762 | Rare:48 | ||||
| chr15:44288621-44288950 | Common:1; Rare:95 | ||||
| chr15:44536858-44537227 | Common:3; Rare:138 | ||||
| chr15:44711368-44711614 | Rare:82; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44729332-44729534 | Common:1; Rare:44 | ||||
| chr15:45402196-45402425 | Common:6; Rare:76 | ||||
| chr15:45587129-45587278 | Rare:30 | ||||
| chr15:45587288-45587628 | Common:1; Rare:115; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:48645645-48645953 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr15:48878007-48878570 | Common:1; Rare:209 |