| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442343-177442519 | Rare:106; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182448851-182449060 | Common:1; Rare:78 | ||||
| chr4:182917319-182917537 | Common:4; Rare:79 | ||||
| chr4:183659122-183659417 | Common:1; Rare:97 | ||||
| chr4:184474512-184474811 | Rare:65 | ||||
| chr4:184649440-184649783 | Common:4; Rare:110 | ||||
| chr4:184734041-184734397 | Common:5; Rare:135 | ||||
| chr4:184805568-184805863 | Common:2; Rare:48 | ||||
| chr4:185396563-185396874 | Rare:104 | ||||
| chr4:185425864-185426273 | Common:4; Rare:126 | ||||
| chr4:185471048-185471425 | Common:10; Rare:51 | ||||
| chr4:185535370-185535668 | Common:2; Rare:108; Clinvar:1; Clinvar (benign):9 | ||||
| chr4:186191599-186191814 | Common:4; Rare:74; Clinvar:1; Clinvar (benign):4 | ||||
| chr4:186723754-186723931 | Common:5; Rare:71 | ||||
| chr4:189940609-189940964 | Common:11; Rare:123 |