| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:43089320-43089508 | Common:3; Rare:61 | ||||
| chr22:43812233-43812500 | Common:4; Rare:90 | ||||
| chr22:43862395-43862660 | Common:8; Rare:109 | ||||
| chr22:43955245-43955562 | Common:4; Rare:98 | ||||
| chr22:44498168-44498479 | Common:2; Rare:119 | ||||
| chr22:45009947-45010140 | Rare:82 | ||||
| chr22:45163675-45164003 | Common:4; Rare:120 | ||||
| chr22:45309676-45309972 | Common:1; Rare:121 | ||||
| chr22:45413575-45413736 | Rare:65 | ||||
| chr22:45671768-45671892 | Common:2; Rare:42 | ||||
| chr22:45671989-45672063 | Rare:35 | ||||
| chr22:46250254-46250417 | Common:3; Rare:51 | ||||
| chr22:46267832-46268037 | Common:1; Rare:62 | ||||
| chr22:46296555-46297102 | Common:5; Rare:158 | ||||
| chr22:46335570-46335836 | Common:6; Rare:119; Clinvar:12; Clinvar (benign):10; Clinvar (pathogenic):1 |