| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:49892856-49893102 | Common:2; Rare:54 | ||||
| chr22:49925329-49925479 | Common:1; Rare:47 | ||||
| chr22:49948699-49948788 | Rare:22 | ||||
| chr22:49949003-49949263 | Common:1; Rare:60 | ||||
| chr22:49971426-49971734 | Common:2; Rare:59 | ||||
| chr22:50194741-50194965 | Rare:63 | ||||
| chr22:50198122-50198390 | Common:1; Rare:106 | ||||
| chr22:50218347-50218441 | Rare:45; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr22:50275622-50275966 | Common:3; Rare:124 | ||||
| chr22:50294096-50294108 | Rare:1 | ||||
| chr22:50300286-50300611 | Common:7; Rare:91 | ||||
| chr22:50314519-50314605 | Common:1; Rare:40 | ||||
| chr22:50461848-50462089 | Rare:94; Clinvar (benign):1 | ||||
| chr22:50465001-50465240 | Common:1; Rare:97; Clinvar (pathogenic):1 | ||||
| chr22:50503509-50503844 | Common:3; Rare:163 |