| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20982201-20982318 | Common:2; Rare:22; Clinvar (benign):2 | ||||
| chr22:21002092-21002195 | Common:3; Rare:35 | ||||
| chr22:21665934-21666059 | Rare:34 | ||||
| chr22:23750979-23751215 | Common:1; Rare:78 | ||||
| chr22:23894325-23894476 | Common:3; Rare:53 | ||||
| chr22:24245076-24245270 | Common:2; Rare:33 | ||||
| chr22:24555629-24556060 | Rare:132 | ||||
| chr22:26483763-26484065 | Common:9; Rare:141; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:26512432-26512570 | Common:2; Rare:60 | ||||
| chr22:27919195-27919518 | Common:5; Rare:144 | ||||
| chr22:28741806-28742078 | Common:2; Rare:79 | ||||
| chr22:28742378-28742701 | Common:1; Rare:83 | ||||
| chr22:28800313-28800694 | Common:6; Rare:137 | ||||
| chr22:29205777-29206031 | Common:1; Rare:69 | ||||
| chr22:29267716-29268339 | Common:3; Rare:174 |