| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:26483781-26483891 | Common:4; Rare:44; Clinvar:4; Clinvar (benign):1 | ||||
| chr22:26512442-26512555 | Common:1; Rare:52 | ||||
| chr22:26590071-26590220 | Common:3; Rare:63 | ||||
| chr22:27919188-27919532 | Common:5; Rare:155 | ||||
| chr22:28741781-28742082 | Common:2; Rare:97; Clinvar:2; Clinvar (benign):5 | ||||
| chr22:28742387-28742683 | Common:1; Rare:73 | ||||
| chr22:28800332-28800750 | Common:5; Rare:152 | ||||
| chr22:29205704-29206108 | Common:1; Rare:99 | ||||
| chr22:29267869-29267933 | Rare:20 | ||||
| chr22:29268153-29268348 | Rare:68 | ||||
| chr22:29581089-29581211 | Common:2; Rare:34 | ||||
| chr22:29767053-29767404 | Common:4; Rare:109 | ||||
| chr22:29767466-29767561 | Common:1; Rare:41 | ||||
| chr22:30265829-30266030 | Rare:48 | ||||
| chr22:30266774-30267029 | Common:1; Rare:59 |