| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:60479050-60479241 | Common:3; Rare:88 | ||||
| chr15:61229214-61229488 | Common:1; Rare:65 | ||||
| chr15:62060364-62060524 | Rare:60 | ||||
| chr15:63042468-63042948 | Common:6; Rare:149; Clinvar:11; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:63048156-63048660 | Common:6; Rare:199; Clinvar:4; Clinvar (benign):4 | ||||
| chr15:63049236-63049489 | Common:1; Rare:62 | ||||
| chr15:63189383-63189614 | Common:2; Rare:79 | ||||
| chr15:63277310-63277626 | Common:4; Rare:63 | ||||
| chr15:63504384-63504663 | Common:2; Rare:93 | ||||
| chr15:63833903-63834053 | Common:1; Rare:60 | ||||
| chr15:64093762-64094091 | Common:1; Rare:95 | ||||
| chr15:64151410-64151752 | Common:1; Rare:100 | ||||
| chr15:64162850-64163279 | Common:5; Rare:147; Clinvar:7; Clinvar (benign):5 | ||||
| chr15:64356140-64356346 | Rare:57 | ||||
| chr15:64387661-64387857 | Common:2; Rare:68 |