| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50251160-50251540 | Common:4; Rare:220 | ||||
| chr22:50260869-50261553 | Common:19; Rare:608 | ||||
| chr22:50261613-50262013 | Common:12; Rare:314 | ||||
| chr22:50269810-50270730 | Common:19; Rare:622 | ||||
| chr22:50306599-50307627 | Common:19; Rare:371 | ||||
| chr22:50318780-50319085 | Common:6; Rare:174 | ||||
| chr22:50319035-50319480 | Common:13; Rare:239 | ||||
| chr22:50326830-50327297 | Common:17; Rare:594 | ||||
| chr22:50327364-50327764 | Common:3; Rare:134 | ||||
| chr22:50342679-50343467 | Common:11; Rare:556 | ||||
| chr22:50474905-50475305 | Common:31; Rare:444 | ||||
| chr22:50481251-50482029 | Common:3; Rare:451 | ||||
| chr22:50507501-50508781 | Common:46; Rare:1571 | ||||
| chr22:50525060-50525400 | Common:4; Rare:121 | ||||
| chr22:50525420-50525900 | Common:30; Rare:834; Clinvar:29; Clinvar (benign):32; Clinvar (pathogenic):2 |