| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:62165278-62165428 | Common:1; Rare:41 | ||||
| chr15:62390422-62390632 | Common:1; Rare:111 | ||||
| chr15:63042505-63042943 | Common:4; Rare:135; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63157417-63157586 | Common:3; Rare:75 | ||||
| chr15:63189295-63189672 | Common:2; Rare:120 | ||||
| chr15:63277241-63277579 | Common:3; Rare:63 | ||||
| chr15:63381677-63381990 | Common:2; Rare:101 | ||||
| chr15:63504373-63504749 | Common:2; Rare:126 | ||||
| chr15:63504801-63504819 | Rare:3 | ||||
| chr15:63833862-63834053 | Common:1; Rare:77 | ||||
| chr15:64093719-64094098 | Common:2; Rare:124 | ||||
| chr15:64095829-64096036 | Common:3; Rare:84 | ||||
| chr15:64162850-64163357 | Common:5; Rare:165; Clinvar:7; Clinvar (benign):5 | ||||
| chr15:64387670-64387877 | Common:2; Rare:78 | ||||
| chr15:64703149-64703310 | Common:1; Rare:63 |