| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696862-121697132 | Common:5; Rare:74 | ||||
| chr4:121801233-121801487 | Common:2; Rare:91; Clinvar (pathogenic):1 | ||||
| chr4:121823818-121824056 | Common:3; Rare:61 | ||||
| chr4:121870413-121870651 | Common:1; Rare:55; Clinvar (benign):1 | ||||
| chr4:122152115-122152390 | Common:2; Rare:93 | ||||
| chr4:122732425-122732762 | Common:1; Rare:105; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922897-122923143 | Common:2; Rare:72 | ||||
| chr4:127632765-127632985 | Common:1; Rare:54 | ||||
| chr4:127880742-127880934 | Common:1; Rare:70 | ||||
| chr4:128060994-128061329 | Common:1; Rare:118 | ||||
| chr4:128287796-128288016 | Common:3; Rare:84 | ||||
| chr4:128288190-128288331 | Common:5; Rare:53 | ||||
| chr4:128811054-128811313 | Rare:51 | ||||
| chr4:129093420-129093736 | Common:2; Rare:90 | ||||
| chr4:129096092-129096174 | Common:1; Rare:19 |