| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:173369778-173369938 | Common:1; Rare:53 | ||||
| chr4:173370687-173371014 | Common:2; Rare:83 | ||||
| chr4:173530168-173530523 | Common:3; Rare:70 | ||||
| chr4:174283617-174283946 | Common:1; Rare:64 | ||||
| chr4:176319721-176320210 | Common:5; Rare:144 | ||||
| chr4:177442362-177442571 | Rare:120; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143824-182143971 | Common:2; Rare:33 | ||||
| chr4:182144438-182144743 | Common:3; Rare:104 | ||||
| chr4:183444469-183444860 | Common:2; Rare:169 | ||||
| chr4:183504385-183504793 | Common:1; Rare:134 | ||||
| chr4:183659160-183659343 | Common:1; Rare:55 | ||||
| chr4:184474501-184474660 | Rare:34 | ||||
| chr4:184649399-184649784 | Common:4; Rare:129 | ||||
| chr4:184734025-184734394 | Common:7; Rare:148 | ||||
| chr4:185203910-185204107 | Common:1; Rare:66 |