| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4248198-4248261 | Common:1; Rare:26 | ||||
| chr4:4290061-4290267 | Common:5; Rare:80 | ||||
| chr4:4541970-4542149 | Common:1; Rare:76 | ||||
| chr4:6640537-6640720 | Common:2; Rare:77 | ||||
| chr4:6987018-6987293 | Common:1; Rare:87 | ||||
| chr4:7068007-7068388 | Common:7; Rare:132 | ||||
| chr4:8440717-8440793 | Rare:27 | ||||
| chr4:10457355-10457472 | Common:2; Rare:46 | ||||
| chr4:15681499-15681869 | Common:3; Rare:126 | ||||
| chr4:17614523-17614651 | Common:2; Rare:50 | ||||
| chr4:17810672-17811061 | Common:4; Rare:127 | ||||
| chr4:20700245-20700486 | Common:1; Rare:105 | ||||
| chr4:24584484-24584698 | Rare:70 | ||||
| chr4:25160411-25160692 | Common:3; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25312585-25312860 | Common:2; Rare:97 |