| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442066-177442291 | Common:1; Rare:85; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr4:177442371-177442605 | Rare:127; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182143886-182144143 | Common:3; Rare:56 | ||||
| chr4:182144168-182144207 | Rare:15 | ||||
| chr4:182144435-182144739 | Common:3; Rare:101 | ||||
| chr4:182448787-182449065 | Common:2; Rare:98 | ||||
| chr4:182917287-182917573 | Common:4; Rare:87 | ||||
| chr4:183444298-183444765 | Common:2; Rare:204 | ||||
| chr4:183504524-183504832 | Common:3; Rare:102 | ||||
| chr4:183506030-183506116 | Rare:30 | ||||
| chr4:183659014-183659417 | Common:1; Rare:121 | ||||
| chr4:184474504-184474838 | Rare:77 | ||||
| chr4:184649399-184649838 | Common:4; Rare:142 | ||||
| chr4:184733360-184733535 | Common:3; Rare:47 | ||||
| chr4:184734016-184734403 | Common:7; Rare:156 |