| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183905175-183905422 | Common:1; Rare:56 | ||||
| chr4:183905791-183905901 | Common:1; Rare:18 | ||||
| chr4:183960124-183960314 | Common:2; Rare:32 | ||||
| chr4:184474524-184474808 | Rare:65 | ||||
| chr4:184648651-184649051 | Common:6; Rare:143 | ||||
| chr4:184649384-184649807 | Common:5; Rare:139 | ||||
| chr4:184733355-184733509 | Common:2; Rare:40 | ||||
| chr4:184734026-184734459 | Common:10; Rare:173 | ||||
| chr4:184825961-184826185 | Common:5; Rare:78 | ||||
| chr4:185143081-185143340 | Common:3; Rare:88; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:185203860-185204400 | Common:7; Rare:155 | ||||
| chr4:185209085-185209254 | Rare:34 | ||||
| chr4:185209371-185209657 | Common:1; Rare:95 | ||||
| chr4:185210117-185210382 | Common:1; Rare:62 | ||||
| chr4:185210510-185210672 | Rare:42 |