| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:67254288-67254480 | Rare:44 | ||||
| chr15:67254488-67254940 | Common:1; Rare:175 | ||||
| chr15:67254970-67255087 | Common:1; Rare:43 | ||||
| chr15:67521054-67521284 | Common:5; Rare:102 | ||||
| chr15:67521505-67521986 | Common:1; Rare:132 | ||||
| chr15:67542028-67542224 | Common:3; Rare:36 | ||||
| chr15:67542500-67542773 | Common:5; Rare:91 | ||||
| chr15:67542939-67543057 | Common:2; Rare:26 | ||||
| chr15:67548718-67549171 | Common:3; Rare:84 | ||||
| chr15:68053981-68054425 | Rare:132 | ||||
| chr15:68054736-68054941 | Common:3; Rare:47 | ||||
| chr15:68229311-68229513 | Common:2; Rare:60; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:68229533-68229920 | Common:5; Rare:151; Clinvar:9; Clinvar (benign):6 | ||||
| chr15:68230013-68230186 | Common:1; Rare:24 | ||||
| chr15:68257138-68257349 | Common:2; Rare:60 |