| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:50687111-50687180 | Rare:18 | ||||
| chr15:50765175-50765567 | Common:3; Rare:125 | ||||
| chr15:50765576-50765876 | Common:2; Rare:103 | ||||
| chr15:50765930-50765995 | Rare:7 | ||||
| chr15:50908360-50908769 | Common:3; Rare:144; Clinvar (benign):2 | ||||
| chr15:50908932-50908962 | Common:1; Rare:7 | ||||
| chr15:50909042-50909403 | Common:3; Rare:81 | ||||
| chr15:51622753-51623081 | Common:3; Rare:114 | ||||
| chr15:51737643-51737750 | Common:1; Rare:37 | ||||
| chr15:51829546-51829896 | Common:1; Rare:93 | ||||
| chr15:51829937-51829999 | Common:2; Rare:8 | ||||
| chr15:51830048-51830173 | Common:1; Rare:39 | ||||
| chr15:51971477-51971982 | Common:2; Rare:175 | ||||
| chr15:52019015-52019320 | Common:2; Rare:153 | ||||
| chr15:52019472-52019546 | Common:1; Rare:23 |