| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:119627990-119628102 | Rare:26 | ||||
| chr4:120066764-120066993 | Common:5; Rare:67 | ||||
| chr4:121696917-121697139 | Common:4; Rare:61 | ||||
| chr4:121801228-121801411 | Common:2; Rare:66 | ||||
| chr4:121823858-121824018 | Common:1; Rare:44 | ||||
| chr4:121870390-121870584 | Common:1; Rare:49; Clinvar (benign):1 | ||||
| chr4:122152219-122152446 | Common:2; Rare:94 | ||||
| chr4:122732432-122732814 | Common:2; Rare:118; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:122922902-122923145 | Common:2; Rare:74; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr4:123396654-123396824 | Rare:41 | ||||
| chr4:123399333-123399653 | Common:1; Rare:98 | ||||
| chr4:124712570-124712884 | Common:1; Rare:86 | ||||
| chr4:127782195-127782361 | Common:2; Rare:50 | ||||
| chr4:127880764-127880934 | Rare:61 | ||||
| chr4:128287789-128287960 | Common:2; Rare:71 |