| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:170553146-170553348 | Common:2; Rare:90 | ||||
| chr6:170554151-170554443 | Common:2; Rare:89 | ||||
| chr6:170584518-170584761 | Common:2; Rare:81 | ||||
| chr7:519166-519294 | Rare:34 | ||||
| chr7:726633-726733 | Rare:34 | ||||
| chr7:727220-727379 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
| chr7:816424-816672 | Common:2; Rare:92 | ||||
| chr7:876225-876785 | Common:8; Rare:236 | ||||
| chr7:975502-975643 | Common:1; Rare:65 | ||||
| chr7:1028296-1028386 | Rare:40 | ||||
| chr7:1138193-1138448 | Common:2; Rare:80 | ||||
| chr7:1504290-1504598 | Common:4; Rare:132 | ||||
| chr7:1530574-1530743 | Common:1; Rare:75 | ||||
| chr7:1537066-1537500 | Common:3; Rare:134 | ||||
| chr7:1537922-1538309 | Common:1; Rare:132 |