| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:109815349-109815817 | Common:2; Rare:121 | ||||
| chr4:110198498-110198792 | Rare:85 | ||||
| chr4:112231580-112231852 | Common:2; Rare:86 | ||||
| chr4:112231948-112232094 | Common:1; Rare:30 | ||||
| chr4:112636829-112637187 | Common:1; Rare:99 | ||||
| chr4:112637394-112637541 | Common:3; Rare:36 | ||||
| chr4:118685196-118685471 | Common:3; Rare:84 | ||||
| chr4:118836005-118836377 | Common:4; Rare:79 | ||||
| chr4:118850176-118850467 | Common:6; Rare:46 | ||||
| chr4:119212510-119212753 | Common:3; Rare:66 | ||||
| chr4:119300536-119300873 | Common:1; Rare:160 | ||||
| chr4:119628673-119629023 | Common:9; Rare:142 | ||||
| chr4:120066700-120066955 | Common:3; Rare:84 | ||||
| chr4:121696869-121697139 | Common:5; Rare:76 | ||||
| chr4:121801213-121801479 | Common:2; Rare:102; Clinvar (pathogenic):1 |