| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173369732-173369935 | Common:1; Rare:64 | ||||
| chr4:173370661-173370976 | Common:2; Rare:81 | ||||
| chr4:173530114-173530523 | Common:3; Rare:80 | ||||
| chr4:174283041-174283332 | Rare:41 | ||||
| chr4:174283601-174283983 | Common:1; Rare:79 | ||||
| chr4:174522359-174522617 | Rare:81; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr4:176277503-176277795 | Common:2; Rare:44 | ||||
| chr4:176319642-176320048 | Common:4; Rare:124 | ||||
| chr4:177442376-177442554 | Rare:105; Clinvar:2 | ||||
| chr4:183504533-183504799 | Common:1; Rare:86 | ||||
| chr4:183659090-183659411 | Common:1; Rare:105 | ||||
| chr4:184649403-184649805 | Common:4; Rare:131 | ||||
| chr4:184734044-184734366 | Common:5; Rare:124 | ||||
| chr4:184805509-184805863 | Common:2; Rare:62 | ||||
| chr4:185143094-185143329 | Common:3; Rare:80; Clinvar:1; Clinvar (benign):3 |