| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:102827755-102828136 | Common:1; Rare:123 | ||||
| chr4:102868880-102869059 | Common:2; Rare:57 | ||||
| chr4:105708626-105708843 | Common:1; Rare:71 | ||||
| chr4:106316191-106316584 | Common:5; Rare:125 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:108650558-108650802 | Rare:82 | ||||
| chr4:109433753-109433867 | Common:1; Rare:44 | ||||
| chr4:112231614-112231844 | Common:2; Rare:72 | ||||
| chr4:112285755-112285966 | Rare:66 | ||||
| chr4:113979634-113979840 | Common:5; Rare:46 | ||||
| chr4:118685321-118685465 | Common:2; Rare:45 | ||||
| chr4:119628669-119628927 | Common:4; Rare:110 | ||||
| chr4:120066769-120066904 | Common:1; Rare:42 | ||||
| chr4:122732470-122732762 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922901-122923109 | Common:2; Rare:49 |