| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72230589-72231724 | Common:28; Rare:1171 | ||||
| chr15:72231748-72232508 | Common:9; Rare:264 | ||||
| chr15:72271847-72272247 | Common:6; Rare:182 | ||||
| chr15:72272448-72273070 | Common:18; Rare:707 | ||||
| chr15:72375540-72375953 | Common:2; Rare:215; Clinvar:9; Clinvar (pathogenic):17 | ||||
| chr15:72375913-72376185 | Common:13; Rare:471; Clinvar:42; Clinvar (benign):8; Clinvar (pathogenic):22 | ||||
| chr15:72376117-72376372 | Common:3; Rare:127; Clinvar:3 | ||||
| chr15:72376474-72376874 | Common:2; Rare:79 | ||||
| chr15:72473580-72473880 | Common:2; Rare:83 | ||||
| chr15:72473890-72474030 | Rare:41 | ||||
| chr15:72474083-72474483 | Rare:571 | ||||
| chr15:72474903-72475398 | Common:4; Rare:331 | ||||
| chr15:72475299-72475448 | Common:3; Rare:69 | ||||
| chr15:72685215-72687036 | Common:22; Rare:843; Clinvar:14; Clinvar (benign):21; Clinvar (pathogenic):3 | ||||
| chr15:72782904-72783497 | Common:3; Rare:186 |