| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70854015-70854263 | Rare:73 | ||||
| chr15:70892403-70892880 | Common:1; Rare:116 | ||||
| chr15:71115387-71115658 | Common:1; Rare:67 | ||||
| chr15:72116848-72116917 | Rare:12 | ||||
| chr15:72117714-72118435 | Common:5; Rare:241 | ||||
| chr15:72118464-72118768 | Common:1; Rare:75 | ||||
| chr15:72204671-72204954 | Rare:45 | ||||
| chr15:72207125-72207455 | Common:2; Rare:62 | ||||
| chr15:72228602-72228802 | Common:1; Rare:52 | ||||
| chr15:72230966-72231028 | Common:2; Rare:22 | ||||
| chr15:72231107-72231542 | Common:3; Rare:142 | ||||
| chr15:72231589-72231643 | Rare:9 | ||||
| chr15:72250070-72250167 | Rare:24 | ||||
| chr15:72272454-72272694 | Rare:59 | ||||
| chr15:72375935-72376173 | Common:3; Rare:93; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):5 |