| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:120066778-120066988 | Common:5; Rare:61 | ||||
| chr4:120922692-120922944 | Rare:72; Clinvar:4 | ||||
| chr4:121696862-121697105 | Common:5; Rare:68 | ||||
| chr4:121801252-121801439 | Common:2; Rare:59 | ||||
| chr4:121870390-121870685 | Common:1; Rare:70; Clinvar (benign):1 | ||||
| chr4:122732392-122732768 | Common:3; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922896-122923144 | Common:2; Rare:73; Clinvar (pathogenic):1 | ||||
| chr4:123399355-123399657 | Common:1; Rare:92 | ||||
| chr4:124712633-124712895 | Common:1; Rare:82 | ||||
| chr4:127782065-127782356 | Common:2; Rare:79 | ||||
| chr4:127880742-127880934 | Common:1; Rare:70 | ||||
| chr4:128060985-128061329 | Common:1; Rare:124 | ||||
| chr4:128287796-128287908 | Common:1; Rare:53 | ||||
| chr4:129093494-129093736 | Rare:73 | ||||
| chr4:133149078-133149329 | Common:2; Rare:76 |