| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:70097904-70098104 | Common:1; Rare:47 | ||||
| chr15:70701935-70702044 | Common:1; Rare:16 | ||||
| chr15:70763367-70763861 | Common:2; Rare:152 | ||||
| chr15:70854101-70854309 | Rare:70 | ||||
| chr15:70892381-70892573 | Common:1; Rare:49 | ||||
| chr15:72118167-72118432 | Common:2; Rare:87 | ||||
| chr15:72231102-72231523 | Common:3; Rare:134 | ||||
| chr15:72231589-72231684 | Common:1; Rare:20 | ||||
| chr15:72272524-72272826 | Common:1; Rare:96 | ||||
| chr15:72375923-72376156 | Common:3; Rare:91; Clinvar:9; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr15:72473984-72473999 | |||||
| chr15:72474174-72474351 | Rare:66 | ||||
| chr15:72686137-72686234 | Common:2; Rare:37; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:73633219-73633561 | Common:1; Rare:132 | ||||
| chr15:73684192-73684414 | Rare:61 |