| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989689-107989868 | Common:3; Rare:78; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:112636869-112637181 | Rare:86 | ||||
| chr4:112637384-112637570 | Common:3; Rare:52 | ||||
| chr4:113293215-113293475 | Common:1; Rare:60; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:113761086-113761276 | Common:1; Rare:52 | ||||
| chr4:113979602-113979837 | Common:6; Rare:53 | ||||
| chr4:118836043-118836325 | Common:3; Rare:60 | ||||
| chr4:119212348-119212738 | Common:4; Rare:122 | ||||
| chr4:120066771-120066863 | Common:1; Rare:30 | ||||
| chr4:121696937-121697154 | Common:4; Rare:60 | ||||
| chr4:121801029-121801422 | Common:4; Rare:119 | ||||
| chr4:122732436-122732700 | Common:1; Rare:77; Clinvar (benign):1 | ||||
| chr4:122922932-122923128 | Common:2; Rare:56 | ||||
| chr4:123399271-123399675 | Common:2; Rare:119 |