| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066758-120066993 | Common:5; Rare:72 | ||||
| chr4:121696944-121697132 | Common:4; Rare:54 | ||||
| chr4:121801221-121801440 | Common:2; Rare:79 | ||||
| chr4:121823824-121824130 | Common:2; Rare:79 | ||||
| chr4:121870413-121870669 | Common:1; Rare:60; Clinvar (benign):1 | ||||
| chr4:122922551-122922689 | Common:2; Rare:63 | ||||
| chr4:122922995-122923148 | Common:1; Rare:56; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:127880736-127880961 | Common:1; Rare:82 | ||||
| chr4:128061000-128061325 | Common:1; Rare:116 | ||||
| chr4:128288205-128288285 | Common:3; Rare:29 | ||||
| chr4:128811332-128811344 | Rare:4 | ||||
| chr4:129093411-129093736 | Common:2; Rare:91 | ||||
| chr4:138242334-138242429 | Rare:26 | ||||
| chr4:139084192-139084554 | Common:4; Rare:157 | ||||
| chr4:139301281-139301625 | Common:4; Rare:104 |