| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:56918416-56918732 | Common:2; Rare:109 | ||||
| chr15:58771028-58771328 | Common:2; Rare:117 | ||||
| chr15:58933557-58933769 | Common:2; Rare:92 | ||||
| chr15:59372546-59372689 | Common:1; Rare:36 | ||||
| chr15:59372843-59373008 | Common:1; Rare:47 | ||||
| chr15:60479037-60479213 | Common:2; Rare:75 | ||||
| chr15:62060361-62060519 | Rare:61 | ||||
| chr15:62835368-62835675 | Common:2; Rare:72 | ||||
| chr15:63042451-63042943 | Common:6; Rare:151; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63157402-63157541 | Common:2; Rare:61 | ||||
| chr15:63504384-63504663 | Common:2; Rare:93 | ||||
| chr15:63597232-63597419 | Common:1; Rare:53 | ||||
| chr15:63597519-63597588 | Rare:26 | ||||
| chr15:64093751-64094091 | Common:1; Rare:103 | ||||
| chr15:64151638-64151757 | Rare:48 |