| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70892347-70892859 | Common:1; Rare:113 | ||||
| chr15:71547228-71547284 | Rare:11 | ||||
| chr15:72117956-72118432 | Common:5; Rare:164 | ||||
| chr15:72231117-72231516 | Common:3; Rare:126 | ||||
| chr15:72375957-72376149 | Common:3; Rare:77; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72474167-72474555 | Rare:137 | ||||
| chr15:72475144-72475250 | Common:1; Rare:28 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783704-72783844 | Common:2; Rare:58 | ||||
| chr15:73684092-73684445 | Rare:96 | ||||
| chr15:73926231-73926466 | Rare:54 | ||||
| chr15:73992176-73992383 | Rare:78 | ||||
| chr15:73994570-73994801 | Common:1; Rare:49 | ||||
| chr15:74128080-74128148 | Rare:10 | ||||
| chr15:74130425-74130586 | Common:2; Rare:29 |