| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24270651-24270973 | Common:3; Rare:118 | ||||
| chr22:24495016-24495416 | Common:7; Rare:139; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:24555030-24555437 | Common:4; Rare:144 | ||||
| chr22:24555854-24556071 | Rare:67 | ||||
| chr22:24627878-24628193 | Common:2; Rare:125 | ||||
| chr22:26483750-26484081 | Common:9; Rare:153; Clinvar:5; Clinvar (benign):2 | ||||
| chr22:26512428-26512550 | Common:1; Rare:55 | ||||
| chr22:26590061-26590247 | Common:3; Rare:79 | ||||
| chr22:27919171-27919528 | Common:5; Rare:156 | ||||
| chr22:28741791-28742103 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
| chr22:28742422-28742709 | Common:1; Rare:66 | ||||
| chr22:28800014-28800750 | Common:7; Rare:251 | ||||
| chr22:29267789-29268348 | Common:2; Rare:160 | ||||
| chr22:29580996-29581211 | Common:2; Rare:72 | ||||
| chr22:29603297-29603663 | Common:3; Rare:81; Clinvar:1 |