| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:63277235-63277641 | Common:4; Rare:93 | ||||
| chr15:63504383-63504734 | Common:2; Rare:122 | ||||
| chr15:63833879-63834064 | Common:1; Rare:71 | ||||
| chr15:64093776-64094092 | Common:1; Rare:88 | ||||
| chr15:64151579-64151752 | Common:1; Rare:62 | ||||
| chr15:64162852-64163279 | Common:5; Rare:145; Clinvar:7; Clinvar (benign):5 | ||||
| chr15:64387648-64387857 | Common:2; Rare:69 | ||||
| chr15:64989762-64990002 | Common:2; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:65286850-65287045 | Rare:62 | ||||
| chr15:65611078-65611390 | Common:2; Rare:107 | ||||
| chr15:65792085-65792470 | Common:1; Rare:109 | ||||
| chr15:66293458-66293629 | Common:4; Rare:53 | ||||
| chr15:66293750-66293880 | Common:2; Rare:38 | ||||
| chr15:66386685-66386950 | Common:2; Rare:104; Clinvar:3; Clinvar (benign):4 | ||||
| chr15:66387064-66387255 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):1 |