| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121801262-121801439 | Common:2; Rare:58 | ||||
| chr4:122152238-122152451 | Common:2; Rare:87 | ||||
| chr4:122732436-122732762 | Common:1; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922933-122923157 | Common:2; Rare:72; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123399328-123399551 | Common:1; Rare:67 | ||||
| chr4:124712566-124712866 | Common:1; Rare:84 | ||||
| chr4:127782225-127782424 | Common:2; Rare:61 | ||||
| chr4:127813228-127813436 | Common:1; Rare:41 | ||||
| chr4:127880789-127880986 | Rare:65 | ||||
| chr4:127965896-127965973 | Common:1; Rare:10; Clinvar (benign):1 | ||||
| chr4:128061002-128061399 | Common:1; Rare:134 | ||||
| chr4:128287789-128288016 | Common:3; Rare:88 | ||||
| chr4:128811062-128811317 | Rare:51 | ||||
| chr4:129093444-129093748 | Common:2; Rare:87 | ||||
| chr4:139177157-139177374 | Rare:58 |