| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72230120-72230720 | Common:4; Rare:158 | ||||
| chr15:72230968-72231598 | Common:14; Rare:501 | ||||
| chr15:72231550-72231653 | Common:1; Rare:22 | ||||
| chr15:72231575-72231792 | Common:3; Rare:73 | ||||
| chr15:72232229-72232629 | Rare:98 | ||||
| chr15:72271620-72272110 | Common:8; Rare:219 | ||||
| chr15:72272438-72273037 | Common:5; Rare:365 | ||||
| chr15:72375490-72375870 | Common:2; Rare:201; Clinvar:5; Clinvar (pathogenic):17 | ||||
| chr15:72375844-72376246 | Common:11; Rare:358; Clinvar:33; Clinvar (benign):6; Clinvar (pathogenic):17 | ||||
| chr15:72474064-72474751 | Common:1; Rare:460 | ||||
| chr15:72474795-72474947 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr15:72475080-72475345 | Common:2; Rare:112 | ||||
| chr15:72475309-72475644 | Common:3; Rare:70 | ||||
| chr15:72686031-72686503 | Common:6; Rare:345; Clinvar:8; Clinvar (benign):16; Clinvar (pathogenic):2 | ||||
| chr15:72782750-72783325 | Common:3; Rare:196 |