| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67125390-67125896 | Common:7; Rare:162 | ||||
| chr15:67128012-67128149 | Rare:28 | ||||
| chr15:67137754-67138236 | Common:10; Rare:301; Clinvar:5; Clinvar (benign):3 | ||||
| chr15:67253802-67254540 | Common:9; Rare:468 | ||||
| chr15:67254503-67255299 | Common:6; Rare:892 | ||||
| chr15:67520336-67520736 | Common:4; Rare:85 | ||||
| chr15:67520752-67521500 | Common:44; Rare:1238 | ||||
| chr15:67521406-67521820 | Common:3; Rare:339 | ||||
| chr15:67521970-67522431 | Common:2; Rare:170 | ||||
| chr15:67542028-67542848 | Common:27; Rare:607 | ||||
| chr15:67542981-67543751 | Common:10; Rare:437 | ||||
| chr15:68053976-68054981 | Common:8; Rare:782 | ||||
| chr15:68205910-68206501 | Common:5; Rare:382 | ||||
| chr15:68229100-68229560 | Common:17; Rare:401; Clinvar:16; Clinvar (benign):12; Clinvar (pathogenic):4 | ||||
| chr15:68229525-68230101 | Common:18; Rare:879; Clinvar:19; Clinvar (benign):21 |