| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50206108-50206299 | Common:1; Rare:57 | ||||
| chr22:50244632-50244662 | Rare:8 | ||||
| chr22:50244949-50245103 | Common:2; Rare:60 | ||||
| chr22:50281701-50281856 | Common:2; Rare:49 | ||||
| chr22:50283352-50283603 | Rare:89 | ||||
| chr22:50525525-50525712 | Common:4; Rare:92; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:50532145-50532265 | Rare:30 | ||||
| chr22:50562876-50563065 | Common:3; Rare:51 | ||||
| chr22:50582806-50583142 | Common:6; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr22:50628038-50628243 | Common:8; Rare:96; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783585-50783854 | Common:2; Rare:90 | ||||
| chr3:3126775-3126990 | Common:4; Rare:94; Clinvar (benign):2 | ||||
| chr3:4303253-4303415 | Common:1; Rare:63 | ||||
| chr3:4493180-4493351 | Rare:62 | ||||
| chr3:4980284-4980526 | Rare:56 |