| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:24270675-24270915 | Common:3; Rare:97 | ||||
| chr22:24555070-24555444 | Common:4; Rare:137 | ||||
| chr22:24555892-24556058 | Rare:50 | ||||
| chr22:24952614-24952717 | Rare:28 | ||||
| chr22:26483757-26483949 | Common:4; Rare:76; Clinvar:5; Clinvar (benign):1 | ||||
| chr22:26512428-26512542 | Common:1; Rare:53 | ||||
| chr22:26590095-26590220 | Common:3; Rare:51 | ||||
| chr22:27919195-27919519 | Common:5; Rare:144 | ||||
| chr22:28741800-28742078 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:29267901-29267938 | Rare:8 | ||||
| chr22:29267955-29268329 | Common:2; Rare:108 | ||||
| chr22:29766947-29767401 | Common:5; Rare:128 | ||||
| chr22:29838187-29838453 | Common:4; Rare:91 | ||||
| chr22:30356868-30356992 | Common:1; Rare:41 | ||||
| chr22:30607104-30607258 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):2 |