| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173530173-173530487 | Common:2; Rare:65 | ||||
| chr4:174283111-174283353 | Rare:34 | ||||
| chr4:174283444-174283965 | Common:2; Rare:95 | ||||
| chr4:174521960-174522177 | Common:4; Rare:55; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:174522199-174522673 | Common:2; Rare:137; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr4:176319721-176320132 | Common:5; Rare:129 | ||||
| chr4:177442072-177442176 | Rare:37 | ||||
| chr4:177442253-177442526 | Common:1; Rare:146; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr4:182917319-182917554 | Common:4; Rare:80 | ||||
| chr4:183504522-183504803 | Common:1; Rare:94 | ||||
| chr4:183658946-183659418 | Common:1; Rare:143 | ||||
| chr4:184474455-184474852 | Rare:87 | ||||
| chr4:184649406-184649805 | Common:4; Rare:129 | ||||
| chr4:184734041-184734419 | Common:6; Rare:145 | ||||
| chr4:184805444-184805835 | Common:1; Rare:72 |