| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:121696850-121697349 | Common:7; Rare:137 | ||||
| chr4:121801215-121801389 | Common:2; Rare:63 | ||||
| chr4:122152228-122152450 | Common:2; Rare:93 | ||||
| chr4:122732425-122732768 | Common:1; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:122922933-122923123 | Common:2; Rare:52 | ||||
| chr4:123396622-123396899 | Rare:66 | ||||
| chr4:123398280-123398474 | Common:1; Rare:67 | ||||
| chr4:123399355-123399653 | Common:1; Rare:91 | ||||
| chr4:127880797-127880913 | Rare:38 | ||||
| chr4:128061000-128061357 | Common:1; Rare:128 | ||||
| chr4:128288172-128288266 | Common:2; Rare:29 | ||||
| chr4:128811136-128811321 | Rare:40 | ||||
| chr4:129093458-129093736 | Common:1; Rare:81 | ||||
| chr4:133149078-133149301 | Common:2; Rare:68 | ||||
| chr4:137532318-137532419 | Common:1; Rare:25 |