| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:127880764-127880940 | Rare:62 | ||||
| chr4:128060968-128061398 | Common:1; Rare:149 | ||||
| chr4:128287799-128288016 | Common:3; Rare:82 | ||||
| chr4:128288155-128288385 | Common:6; Rare:85 | ||||
| chr4:128811222-128811273 | Rare:11 | ||||
| chr4:129093411-129093712 | Common:2; Rare:87 | ||||
| chr4:133149099-133149295 | Common:2; Rare:57 | ||||
| chr4:138242240-138242646 | Common:1; Rare:86 | ||||
| chr4:139015455-139015782 | Common:2; Rare:102 | ||||
| chr4:139084192-139084544 | Common:4; Rare:156 | ||||
| chr4:139301218-139301759 | Common:5; Rare:156 | ||||
| chr4:139453659-139454190 | Common:5; Rare:149; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:139556135-139556289 | Rare:32 | ||||
| chr4:139556391-139556622 | Rare:32 | ||||
| chr4:140373344-140373732 | Common:3; Rare:152 |