| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:112637380-112637570 | Common:3; Rare:53 | ||||
| chr4:113761107-113761373 | Common:1; Rare:62 | ||||
| chr4:118685339-118685463 | Common:2; Rare:40 | ||||
| chr4:118836036-118836348 | Common:3; Rare:68 | ||||
| chr4:118888763-118888998 | Common:1; Rare:63 | ||||
| chr4:119212513-119212757 | Common:3; Rare:65 | ||||
| chr4:119213027-119213330 | Rare:50 | ||||
| chr4:119300484-119300931 | Common:2; Rare:198 | ||||
| chr4:119628043-119628102 | Rare:16 | ||||
| chr4:120066825-120066955 | Common:3; Rare:36 | ||||
| chr4:121696862-121697139 | Common:5; Rare:76 | ||||
| chr4:121801263-121801405 | Common:2; Rare:47 | ||||
| chr4:122152249-122152458 | Common:2; Rare:83 | ||||
| chr4:122732417-122732768 | Common:2; Rare:108; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922942-122923139 | Common:2; Rare:62 |