| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31736384-31736685 | Common:2; Rare:54 | ||||
| chr6:31739686-31740032 | Common:3; Rare:90 | ||||
| chr6:31806786-31807075 | Common:3; Rare:116 | ||||
| chr6:31815350-31815555 | Common:1; Rare:67 | ||||
| chr6:31834584-31834929 | Common:3; Rare:79 | ||||
| chr6:31897673-31897782 | Rare:20 | ||||
| chr6:31958891-31959188 | Rare:93; Clinvar:8 | ||||
| chr6:32176056-32176248 | Common:1; Rare:38 | ||||
| chr6:32843986-32844119 | Rare:31; Clinvar:1 | ||||
| chr6:32844622-32844840 | Common:1; Rare:47 | ||||
| chr6:32853670-32853758 | Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32853979-32854209 | Common:2; Rare:55 | ||||
| chr6:33200656-33200938 | Common:2; Rare:85 | ||||
| chr6:33208443-33208522 | Rare:22 | ||||
| chr6:33271678-33272122 | Common:2; Rare:156 |