| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:20982204-20982347 | Common:2; Rare:30; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:21002106-21002220 | Common:3; Rare:38 | ||||
| chr22:23767931-23768019 | Rare:23 | ||||
| chr22:23857793-23857949 | Common:3; Rare:52 | ||||
| chr22:23894598-23894833 | Common:3; Rare:85 | ||||
| chr22:24555018-24555487 | Common:4; Rare:172 | ||||
| chr22:24555617-24556026 | Rare:126 | ||||
| chr22:26483781-26483909 | Common:4; Rare:49; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:26512436-26512551 | Common:1; Rare:52 | ||||
| chr22:26590074-26590220 | Common:3; Rare:60 | ||||
| chr22:27919188-27919518 | Common:5; Rare:147 | ||||
| chr22:28741777-28742080 | Common:2; Rare:98; Clinvar:2; Clinvar (benign):7 | ||||
| chr22:28800485-28800696 | Common:5; Rare:88 | ||||
| chr22:29267825-29267996 | Rare:42 | ||||
| chr22:29268152-29268336 | Rare:67 |