| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32176054-32176244 | Common:1; Rare:39 | ||||
| chr6:32178092-32178508 | Common:2; Rare:69 | ||||
| chr6:32190165-32190319 | Rare:30 | ||||
| chr6:32530285-32530533 | Common:16; Rare:7 | ||||
| chr6:32838212-32838329 | Rare:31; Clinvar (benign):1 | ||||
| chr6:32844009-32844144 | Rare:30; Clinvar:1 | ||||
| chr6:32844622-32844840 | Common:1; Rare:47 | ||||
| chr6:32853670-32853782 | Rare:49; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32853989-32854216 | Common:2; Rare:52 | ||||
| chr6:32968819-32968924 | Common:4; Rare:34 | ||||
| chr6:33075812-33076026 | Common:2; Rare:26 | ||||
| chr6:33200359-33200443 | Rare:22 | ||||
| chr6:33200656-33200925 | Common:2; Rare:82 | ||||
| chr6:33271678-33272122 | Common:2; Rare:156 | ||||
| chr6:33272341-33272723 | Rare:74 |