| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173369807-173369935 | Common:1; Rare:44 | ||||
| chr4:173370674-173370961 | Common:2; Rare:72 | ||||
| chr4:174283659-174283965 | Common:1; Rare:59 | ||||
| chr4:176319718-176320055 | Common:4; Rare:115 | ||||
| chr4:177442377-177442521 | Rare:86; Clinvar:2 | ||||
| chr4:182143819-182143963 | Common:2; Rare:32 | ||||
| chr4:182144435-182144731 | Common:3; Rare:95 | ||||
| chr4:182448753-182449083 | Common:2; Rare:116 | ||||
| chr4:182917306-182917547 | Common:4; Rare:81 | ||||
| chr4:183504520-183504792 | Common:1; Rare:91 | ||||
| chr4:183659122-183659349 | Common:1; Rare:72 | ||||
| chr4:184474519-184474716 | Rare:49 | ||||
| chr4:184649396-184649775 | Common:5; Rare:126 | ||||
| chr4:185143136-185143315 | Common:2; Rare:61; Clinvar (benign):3 | ||||
| chr4:185203915-185204097 | Rare:62 |