| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72231094-72231520 | Common:3; Rare:135 | ||||
| chr15:72375935-72376129 | Common:2; Rare:79; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72686147-72686220 | Common:2; Rare:28; Clinvar:2; Clinvar (benign):2 | ||||
| chr15:72783629-72783881 | Common:2; Rare:114 | ||||
| chr15:73633123-73633595 | Common:2; Rare:181 | ||||
| chr15:73684205-73684460 | Rare:70 | ||||
| chr15:73926294-73926475 | Rare:50 | ||||
| chr15:73994581-73994761 | Common:1; Rare:34 | ||||
| chr15:74041605-74041639 | Rare:4 | ||||
| chr15:74173540-74173862 | Common:2; Rare:73 | ||||
| chr15:74174320-74174593 | Common:3; Rare:53 | ||||
| chr15:74202424-74202709 | Common:2; Rare:59 | ||||
| chr15:74202711-74203049 | Common:1; Rare:81; Clinvar:2 | ||||
| chr15:74461079-74461298 | Common:1; Rare:70 | ||||
| chr15:74540966-74541276 | Common:4; Rare:109 |