| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67065244-67066135 | Common:7; Rare:667; Clinvar:6; Clinvar (benign):3 | ||||
| chr15:67125600-67125913 | Common:5; Rare:96 | ||||
| chr15:67254279-67254919 | Common:3; Rare:505 | ||||
| chr15:67520865-67521371 | Common:18; Rare:449 | ||||
| chr15:67521330-67521500 | Rare:123 | ||||
| chr15:67521549-67521838 | Rare:169 | ||||
| chr15:67542467-67542857 | Common:9; Rare:298 | ||||
| chr15:68054016-68054395 | Rare:292 | ||||
| chr15:68054570-68055123 | Common:10; Rare:237 | ||||
| chr15:68229325-68229544 | Common:2; Rare:113; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:68229562-68229899 | Common:6; Rare:232; Clinvar:7; Clinvar (benign):8 | ||||
| chr15:68257082-68257361 | Common:5; Rare:121 | ||||
| chr15:68277019-68277419 | Rare:107 | ||||
| chr15:68277583-68278198 | Common:20; Rare:470 | ||||
| chr15:68278170-68278599 | Common:4; Rare:220 |