| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989690-107989935 | Common:5; Rare:111; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620380-108620736 | Common:6; Rare:154 | ||||
| chr4:109433738-109433946 | Common:1; Rare:67 | ||||
| chr4:109560088-109560357 | Common:3; Rare:76 | ||||
| chr4:109729953-109730249 | Common:4; Rare:82 | ||||
| chr4:109815475-109815553 | Rare:25 | ||||
| chr4:112231958-112232041 | Rare:21 | ||||
| chr4:112285738-112286002 | Rare:83 | ||||
| chr4:112636886-112637187 | Common:1; Rare:84 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:118352380-118352533 | Rare:52; Clinvar:3 | ||||
| chr4:119212500-119212812 | Common:4; Rare:82 | ||||
| chr4:119300521-119300960 | Common:2; Rare:184 | ||||
| chr4:119628764-119628949 | Common:3; Rare:79 | ||||
| chr4:120066775-120066913 | Common:2; Rare:42 |