| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:50192541-50192649 | Common:1; Rare:25 | ||||
| chr22:50200706-50201118 | Common:6; Rare:148 | ||||
| chr22:50244480-50244680 | Common:1; Rare:62 | ||||
| chr22:50244939-50245153 | Common:2; Rare:81 | ||||
| chr22:50251178-50251389 | Common:1; Rare:71 | ||||
| chr22:50261158-50261421 | Common:3; Rare:100 | ||||
| chr22:50270026-50270192 | Common:2; Rare:47 | ||||
| chr22:50307545-50308016 | Common:11; Rare:108 | ||||
| chr22:50326966-50327270 | Common:3; Rare:104 | ||||
| chr22:50343164-50343416 | Common:2; Rare:106 | ||||
| chr22:50475005-50475263 | Common:6; Rare:77 | ||||
| chr22:50507628-50507991 | Common:1; Rare:100 | ||||
| chr22:50508085-50508338 | Common:3; Rare:93 | ||||
| chr22:50525489-50525842 | Common:7; Rare:189; Clinvar:7; Clinvar (benign):9 | ||||
| chr22:50526125-50526411 | Common:2; Rare:151; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):4 |