| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112285761-112286002 | Rare:74 | ||||
| chr4:112636836-112637193 | Common:1; Rare:99 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:113761107-113761243 | Common:1; Rare:37 | ||||
| chr4:118685318-118685541 | Common:2; Rare:62 | ||||
| chr4:118835952-118836218 | Common:1; Rare:60 | ||||
| chr4:119212410-119212756 | Common:3; Rare:104 | ||||
| chr4:119212995-119213191 | Common:1; Rare:38 | ||||
| chr4:119300497-119300928 | Common:2; Rare:190 | ||||
| chr4:120066754-120066988 | Common:5; Rare:70 | ||||
| chr4:121696858-121697243 | Common:6; Rare:112 | ||||
| chr4:121801233-121801411 | Common:2; Rare:62 | ||||
| chr4:121823487-121823525 | Rare:14 | ||||
| chr4:121823858-121824121 | Common:2; Rare:68 | ||||
| chr4:122732432-122732769 | Common:1; Rare:101; Clinvar:2; Clinvar (benign):1 |