| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74615594-74615907 | Common:4; Rare:101 | ||||
| chr15:74695927-74696098 | Rare:58 | ||||
| chr15:74843085-74843433 | Common:2; Rare:99 | ||||
| chr15:74872935-74873109 | Rare:38 | ||||
| chr15:74873274-74873447 | Common:5; Rare:59 | ||||
| chr15:74889953-74890104 | Rare:62; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74906600-74906871 | Common:2; Rare:99 | ||||
| chr15:74937966-74938254 | Common:2; Rare:93 | ||||
| chr15:74995276-74995656 | Common:8; Rare:127 | ||||
| chr15:75195558-75195673 | Rare:23 | ||||
| chr15:75335971-75336089 | Common:1; Rare:51 | ||||
| chr15:75455802-75455967 | Rare:51 | ||||
| chr15:75579237-75579538 | Common:2; Rare:87 | ||||
| chr15:75625599-75625907 | Common:2; Rare:73 | ||||
| chr15:75640159-75640380 | Common:1; Rare:77 |