| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231018-72231742 | Common:6; Rare:220 | ||||
| chr15:72272302-72272341 | Rare:6 | ||||
| chr15:72272455-72272992 | Common:3; Rare:137 | ||||
| chr15:72375900-72376285 | Common:4; Rare:145; Clinvar:12; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473624-72473869 | Common:1; Rare:41 | ||||
| chr15:72474040-72474434 | Rare:132 | ||||
| chr15:72475086-72475475 | Common:4; Rare:106 | ||||
| chr15:72685903-72686311 | Common:3; Rare:127; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72782961-72783368 | Common:2; Rare:102 | ||||
| chr15:72783474-72784185 | Common:4; Rare:236 | ||||
| chr15:73051733-73051912 | Common:1; Rare:48 | ||||
| chr15:73051935-73051945 | Rare:4 | ||||
| chr15:73633208-73633695 | Common:4; Rare:176 | ||||
| chr15:73992202-73992520 | Common:3; Rare:108 | ||||
| chr15:73994506-73994855 | Common:2; Rare:85 |