| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31630780-31630980 | Common:5; Rare:56 | ||||
| chr22:31638305-31638654 | Common:3; Rare:60 | ||||
| chr22:31661930-31662031 | Common:1; Rare:32 | ||||
| chr22:31662153-31662441 | Common:2; Rare:108 | ||||
| chr22:31749633-31749756 | Rare:32 | ||||
| chr22:31750022-31750385 | Common:3; Rare:104 | ||||
| chr22:31753677-31754190 | Common:1; Rare:166 | ||||
| chr22:31754407-31754557 | Common:1; Rare:29 | ||||
| chr22:31943931-31944095 | Common:4; Rare:41 | ||||
| chr22:31944224-31944578 | Common:5; Rare:136 | ||||
| chr22:31944911-31945023 | Common:1; Rare:39 | ||||
| chr22:32412157-32412326 | Common:2; Rare:51 | ||||
| chr22:32474565-32474911 | Common:5; Rare:108; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:32474948-32475114 | Rare:60 | ||||
| chr22:32475266-32475420 | Common:2; Rare:67; Clinvar (benign):1 |