| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:76594120-76594447 | Common:1; Rare:64 | ||||
| chr6:76757569-76757738 | Common:6; Rare:30 | ||||
| chr6:76877079-76877205 | Common:2; Rare:28 | ||||
| chr6:77663705-77663769 | Rare:22 | ||||
| chr6:77665084-77665153 | Common:1; Rare:18 | ||||
| chr6:78941158-78941548 | Common:1; Rare:81 | ||||
| chr6:79152333-79152642 | Common:2; Rare:61 | ||||
| chr6:79201756-79201814 | Rare:14 | ||||
| chr6:79201941-79202212 | Rare:61 | ||||
| chr6:79233613-79233844 | Common:3; Rare:53 | ||||
| chr6:79233902-79233971 | Rare:18 | ||||
| chr6:80465875-80465891 | Rare:2 | ||||
| chr6:80513111-80513170 | Rare:19 | ||||
| chr6:82959414-82959705 | Rare:48 | ||||
| chr6:83854118-83854330 | Common:1; Rare:45; Clinvar (pathogenic):1 |