| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:21665965-21666070 | Rare:34 | ||||
| chr22:22508678-22508902 | Common:1; Rare:82 | ||||
| chr22:23750933-23751130 | Common:3; Rare:67 | ||||
| chr22:23857666-23857916 | Common:2; Rare:87 | ||||
| chr22:23894311-23894568 | Common:3; Rare:96 | ||||
| chr22:23894578-23894915 | Common:3; Rare:136; Clinvar:1 | ||||
| chr22:24011209-24011484 | Rare:93 | ||||
| chr22:24155964-24156008 | Rare:12 | ||||
| chr22:24270632-24270951 | Common:3; Rare:115 | ||||
| chr22:24555080-24555437 | Common:3; Rare:129 | ||||
| chr22:24555884-24556071 | Rare:55 | ||||
| chr22:24806140-24806311 | Common:1; Rare:66 | ||||
| chr22:24952593-24952732 | Rare:40 | ||||
| chr22:25564765-25564989 | Common:1; Rare:101 | ||||
| chr22:26483752-26484036 | Common:7; Rare:133; Clinvar:5; Clinvar (benign):1 |