| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4248203-4248276 | Common:1; Rare:30 | ||||
| chr4:4290117-4290277 | Common:3; Rare:64 | ||||
| chr4:4541970-4542149 | Common:1; Rare:76 | ||||
| chr4:6640531-6640720 | Common:2; Rare:79 | ||||
| chr4:6987006-6987303 | Common:2; Rare:94 | ||||
| chr4:7068025-7068341 | Common:3; Rare:105 | ||||
| chr4:8440717-8440984 | Rare:100 | ||||
| chr4:10116666-10117089 | Common:8; Rare:198 | ||||
| chr4:15655289-15655455 | Common:1; Rare:74 | ||||
| chr4:15681499-15681875 | Common:4; Rare:129 | ||||
| chr4:17577281-17577550 | Common:1; Rare:125 | ||||
| chr4:17614551-17614651 | Common:2; Rare:43 | ||||
| chr4:17810664-17811013 | Common:2; Rare:112 | ||||
| chr4:24584473-24584763 | Common:1; Rare:84 | ||||
| chr4:25160382-25160704 | Common:3; Rare:93; Clinvar:2; Clinvar (benign):1 |