| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:64989732-64990167 | Common:27; Rare:653; Clinvar:12; Clinvar (benign):5 | ||||
| chr15:64990172-64990572 | Common:2; Rare:77 | ||||
| chr15:65028896-65029296 | Common:5; Rare:83 | ||||
| chr15:65029440-65029850 | Common:12; Rare:266; Clinvar:6; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr15:65133420-65133700 | Common:1; Rare:132 | ||||
| chr15:65133710-65134130 | Common:7; Rare:456 | ||||
| chr15:65184139-65184881 | Common:2; Rare:257 | ||||
| chr15:65184919-65185163 | Common:8; Rare:191 | ||||
| chr15:65185185-65185879 | Common:10; Rare:802 | ||||
| chr15:65285866-65286581 | Common:2; Rare:429 | ||||
| chr15:65286732-65287132 | Rare:490 | ||||
| chr15:65385660-65385950 | Common:2; Rare:83 | ||||
| chr15:65421975-65422736 | Common:6; Rare:248 | ||||
| chr15:65422984-65423832 | Common:2; Rare:226 | ||||
| chr15:65516980-65517968 | Common:28; Rare:1131 |