| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:77819908-77820024 | Common:1; Rare:24 | ||||
| chr4:77820104-77820477 | Rare:449 | ||||
| chr4:77861855-77862255 | Common:2; Rare:120 | ||||
| chr4:77862204-77863100 | Common:27; Rare:953 | ||||
| chr4:77863019-77863163 | Rare:30 | ||||
| chr4:78551251-78552180 | Common:11; Rare:450 | ||||
| chr4:78552358-78552758 | Common:6; Rare:63 | ||||
| chr4:78775700-78777246 | Common:25; Rare:2147 | ||||
| chr4:78939220-78939659 | Common:14; Rare:828 | ||||
| chr4:79325189-79325837 | Common:5; Rare:286 | ||||
| chr4:79325896-79326320 | Common:7; Rare:450 | ||||
| chr4:80070847-80071475 | Common:1; Rare:117 | ||||
| chr4:80071438-80072460 | Common:10; Rare:409 | ||||
| chr4:80072480-80073854 | Common:30; Rare:1119; Clinvar:18; Clinvar (benign):14 | ||||
| chr4:80125032-80126113 | Common:14; Rare:486 |