| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67521554-67521753 | Rare:55 | ||||
| chr15:67521950-67521996 | Rare:13 | ||||
| chr15:67542522-67542782 | Common:4; Rare:91 | ||||
| chr15:67542833-67542843 | Rare:2 | ||||
| chr15:68053952-68054490 | Rare:153 | ||||
| chr15:68054736-68054950 | Common:3; Rare:49 | ||||
| chr15:68205264-68205476 | Rare:75 | ||||
| chr15:68229333-68229563 | Common:2; Rare:72; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr15:68229574-68229932 | Common:4; Rare:137; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:68277182-68277400 | Rare:45 | ||||
| chr15:68277420-68278254 | Common:12; Rare:260 | ||||
| chr15:68278257-68278412 | Rare:46 | ||||
| chr15:68432182-68432280 | Common:1; Rare:22 | ||||
| chr15:68787919-68787996 | Rare:23 | ||||
| chr15:68817605-68817794 | Common:2; Rare:59 |