| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:69414198-69414429 | Rare:72 | ||||
| chr15:69452725-69452896 | Common:4; Rare:78 | ||||
| chr15:70097879-70098092 | Common:1; Rare:48 | ||||
| chr15:70763431-70763840 | Common:2; Rare:135 | ||||
| chr15:70892353-70892855 | Common:1; Rare:110 | ||||
| chr15:72118167-72118432 | Common:2; Rare:87 | ||||
| chr15:72231122-72231548 | Common:3; Rare:141 | ||||
| chr15:72375968-72376129 | Common:1; Rare:64; Clinvar:5; Clinvar (pathogenic):2 | ||||
| chr15:72685954-72686234 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:73633232-73633305 | Rare:31 | ||||
| chr15:74461107-74461329 | Rare:65 | ||||
| chr15:74540901-74541296 | Common:6; Rare:139 | ||||
| chr15:74615559-74615891 | Common:4; Rare:106 | ||||
| chr15:74695963-74696076 | Rare:41 | ||||
| chr15:74873321-74873481 | Common:5; Rare:47 |