| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:66504786-66505140 | Common:1; Rare:135 | ||||
| chr15:67254603-67254818 | Common:1; Rare:85 | ||||
| chr15:69414201-69414453 | Rare:85 | ||||
| chr15:72231117-72231516 | Common:3; Rare:126 | ||||
| chr15:72375958-72376129 | Common:2; Rare:71; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:72686157-72686220 | Common:2; Rare:24; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:73633232-73633587 | Common:2; Rare:138 | ||||
| chr15:74202770-74203047 | Common:1; Rare:70; Clinvar:2 | ||||
| chr15:74461107-74461298 | Rare:61 | ||||
| chr15:74873321-74873488 | Common:6; Rare:49 | ||||
| chr15:75335967-75336106 | Common:1; Rare:65 | ||||
| chr15:75368585-75368644 | Rare:26 | ||||
| chr15:75625686-75625821 | Common:1; Rare:33 | ||||
| chr15:75903812-75903956 | Rare:58 | ||||
| chr15:76905333-76905494 | Common:1; Rare:58 |