| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75514273-75514505 | Common:1; Rare:80 | ||||
| chr4:75673088-75673222 | Rare:31 | ||||
| chr4:75673264-75673692 | Common:1; Rare:163 | ||||
| chr4:75724357-75724730 | Common:1; Rare:101 | ||||
| chr4:75940286-75940435 | Common:1; Rare:36 | ||||
| chr4:76148370-76148579 | Common:3; Rare:64 | ||||
| chr4:76213467-76213988 | Common:5; Rare:175; Clinvar:2; Clinvar (benign):8 | ||||
| chr4:76949536-76949869 | Common:2; Rare:104 | ||||
| chr4:77075965-77076057 | Rare:52 | ||||
| chr4:77862716-77862879 | Common:1; Rare:73 | ||||
| chr4:78939246-78939519 | Common:2; Rare:115 | ||||
| chr4:80072556-80072831 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:80073037-80073267 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:82373936-82374317 | Common:3; Rare:116 | ||||
| chr4:82429377-82429562 | Rare:114; Clinvar:5; Clinvar (benign):3 |