| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:72473681-72474036 | Common:1; Rare:65 | ||||
| chr15:72474131-72474704 | Rare:198 | ||||
| chr15:72474725-72475009 | Common:1; Rare:89; Clinvar (benign):1 | ||||
| chr15:72475077-72475512 | Common:4; Rare:117 | ||||
| chr15:72685581-72685783 | Common:2; Rare:37 | ||||
| chr15:72685892-72686031 | Common:1; Rare:29 | ||||
| chr15:72686037-72686586 | Common:2; Rare:165; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr15:72686634-72686785 | Common:1; Rare:23 | ||||
| chr15:72783009-72783363 | Common:2; Rare:83 | ||||
| chr15:72783424-72783539 | Rare:30 | ||||
| chr15:72783681-72784180 | Common:4; Rare:160 | ||||
| chr15:73051333-73051463 | Rare:27 | ||||
| chr15:73051561-73051787 | Common:1; Rare:66 | ||||
| chr15:73051822-73051939 | Common:1; Rare:38 | ||||
| chr15:73052047-73052676 | Common:4; Rare:176 |