| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70892381-70892479 | Rare:28 | ||||
| chr15:72118168-72118432 | Common:2; Rare:86 | ||||
| chr15:72231117-72231511 | Common:3; Rare:123 | ||||
| chr15:72375957-72376103 | Common:2; Rare:63; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr15:73633265-73633555 | Common:1; Rare:103 | ||||
| chr15:73926322-73926466 | Rare:40 | ||||
| chr15:73994587-73994792 | Rare:44 | ||||
| chr15:74461101-74461298 | Rare:63 | ||||
| chr15:74540966-74541257 | Common:3; Rare:102 | ||||
| chr15:74615678-74615883 | Common:3; Rare:63 | ||||
| chr15:74843119-74843296 | Common:1; Rare:55 | ||||
| chr15:75335954-75336103 | Common:1; Rare:72 | ||||
| chr15:75625607-75625821 | Common:2; Rare:51 | ||||
| chr15:76311351-76311630 | Common:1; Rare:95; Clinvar:6; Clinvar (benign):8 | ||||
| chr15:76905308-76905477 | Common:1; Rare:60 |