| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:46053778-46053901 | Rare:43 | ||||
| chr22:46250254-46250438 | Common:3; Rare:62 | ||||
| chr22:46267832-46268048 | Common:1; Rare:69 | ||||
| chr22:46296711-46296918 | Common:2; Rare:75 | ||||
| chr22:46335621-46335809 | Common:5; Rare:88; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr22:46693428-46693717 | Rare:69 | ||||
| chr22:46762447-46762713 | Common:3; Rare:102 | ||||
| chr22:49918373-49918805 | Common:5; Rare:157; Clinvar (benign):1 | ||||
| chr22:50185703-50186008 | Common:5; Rare:117 | ||||
| chr22:50190273-50190619 | Common:4; Rare:101 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50454858-50455067 | Rare:85; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:50481548-50481855 | Common:3; Rare:88 | ||||
| chr22:50487133-50487221 | Rare:21 | ||||
| chr22:50506105-50506394 | Rare:137 |