| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121823763-121824075 | Common:4; Rare:76 | ||||
| chr4:121870390-121870669 | Common:1; Rare:67; Clinvar (benign):1 | ||||
| chr4:122152261-122152416 | Common:2; Rare:68 | ||||
| chr4:122732432-122732791 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922932-122923184 | Common:2; Rare:79; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:124712626-124713122 | Common:2; Rare:147 | ||||
| chr4:127632764-127633082 | Common:1; Rare:89 | ||||
| chr4:127782205-127782381 | Common:2; Rare:61 | ||||
| chr4:127880760-127880956 | Rare:69 | ||||
| chr4:127881467-127881631 | Rare:35 | ||||
| chr4:128060947-128061329 | Common:1; Rare:137 | ||||
| chr4:128287796-128287907 | Common:1; Rare:53 | ||||
| chr4:128288190-128288331 | Common:5; Rare:53 | ||||
| chr4:128811174-128811317 | Rare:30 | ||||
| chr4:129093355-129093753 | Common:2; Rare:106 |