| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67542015-67542259 | Common:3; Rare:41 | ||||
| chr15:67542462-67542879 | Common:6; Rare:126 | ||||
| chr15:67543567-67543709 | Common:1; Rare:16 | ||||
| chr15:68053981-68054390 | Rare:117 | ||||
| chr15:68054718-68054818 | Common:3; Rare:23 | ||||
| chr15:68229165-68229566 | Common:5; Rare:121; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:68229625-68229903 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:68277192-68277479 | Common:1; Rare:68 | ||||
| chr15:68277551-68278334 | Common:10; Rare:243 | ||||
| chr15:68817405-68817584 | Rare:50 | ||||
| chr15:68817599-68818000 | Common:3; Rare:118 | ||||
| chr15:68818144-68818294 | Common:1; Rare:59 | ||||
| chr15:68818522-68818938 | Common:4; Rare:132 | ||||
| chr15:68820375-68820530 | Rare:33 | ||||
| chr15:68820761-68821178 | Rare:127 |