| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:68817605-68817701 | Common:1; Rare:36 | ||||
| chr15:68820726-68821046 | Rare:97 | ||||
| chr15:69452688-69453020 | Common:5; Rare:139 | ||||
| chr15:70096256-70096381 | Rare:36 | ||||
| chr15:70763364-70763840 | Common:2; Rare:150 | ||||
| chr15:70854101-70854289 | Rare:62 | ||||
| chr15:70892403-70892871 | Common:1; Rare:111 | ||||
| chr15:72118010-72118426 | Common:3; Rare:143 | ||||
| chr15:72230219-72230552 | Common:2; Rare:97 | ||||
| chr15:72231107-72231318 | Common:1; Rare:75 | ||||
| chr15:72231330-72231520 | Common:2; Rare:55 | ||||
| chr15:72375953-72376129 | Common:2; Rare:73; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474195-72474642 | Rare:159 | ||||
| chr15:72474741-72474992 | Common:1; Rare:82; Clinvar (benign):1 | ||||
| chr15:72475144-72475260 | Common:1; Rare:30 |