| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:122733256-122733656 | Common:10; Rare:98 | ||||
| chr4:122826190-122826883 | Common:14; Rare:652 | ||||
| chr4:122826900-122827170 | Common:3; Rare:86; Clinvar (benign):1 | ||||
| chr4:122827205-122827605 | Common:9; Rare:191 | ||||
| chr4:122921708-122922810 | Common:26; Rare:1049 | ||||
| chr4:122922828-122923214 | Common:13; Rare:573; Clinvar:6; Clinvar (pathogenic):6 | ||||
| chr4:122923223-122923623 | Common:4; Rare:138 | ||||
| chr4:123396552-123396952 | Rare:182 | ||||
| chr4:123397195-123397666 | Common:1; Rare:193 | ||||
| chr4:123398210-123398885 | Common:4; Rare:297 | ||||
| chr4:124712120-124712511 | Common:1; Rare:191 | ||||
| chr4:124712616-124713160 | Common:8; Rare:723 | ||||
| chr4:127632663-127633399 | Common:7; Rare:367 | ||||
| chr4:127633372-127633821 | Common:1; Rare:140 | ||||
| chr4:127781960-127782390 | Common:12; Rare:600 |