| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066420-120066481 | Rare:12 | ||||
| chr4:120066730-120067005 | Common:5; Rare:85 | ||||
| chr4:120067190-120067506 | Common:5; Rare:71 | ||||
| chr4:120922828-120923062 | Common:1; Rare:69; Clinvar:1 | ||||
| chr4:121156835-121157419 | Common:8; Rare:152 | ||||
| chr4:121696885-121697130 | Common:5; Rare:70 | ||||
| chr4:121801213-121801488 | Common:2; Rare:105; Clinvar (pathogenic):1 | ||||
| chr4:121823499-121823525 | Rare:8 | ||||
| chr4:121823767-121824121 | Common:4; Rare:88 | ||||
| chr4:121870406-121870651 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr4:122152268-122152390 | Common:2; Rare:53 | ||||
| chr4:122732417-122732785 | Common:3; Rare:115; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:122922467-122922672 | Common:3; Rare:100 | ||||
| chr4:122922896-122923222 | Common:2; Rare:99; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:122923356-122923453 | Rare:17 |