| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32844002-32844119 | Rare:26; Clinvar:1 | ||||
| chr6:32844372-32844508 | Rare:33 | ||||
| chr6:32844652-32844840 | Common:1; Rare:39 | ||||
| chr6:32854022-32854228 | Common:2; Rare:54 | ||||
| chr6:32968809-32968945 | Common:4; Rare:40 | ||||
| chr6:32977529-32977833 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr6:33200356-33200422 | Rare:17 | ||||
| chr6:33200654-33200925 | Common:2; Rare:82 | ||||
| chr6:33271840-33272122 | Common:1; Rare:118 | ||||
| chr6:33277043-33277176 | Common:2; Rare:40 | ||||
| chr6:33289481-33289632 | Common:1; Rare:33 | ||||
| chr6:33298914-33299064 | Rare:40 | ||||
| chr6:33299182-33299489 | Common:3; Rare:63 | ||||
| chr6:33391574-33391881 | Common:2; Rare:71 | ||||
| chr6:33410901-33411062 | Rare:31 |