| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32177079-32177192 | Rare:23 | ||||
| chr6:32190146-32190295 | Rare:30 | ||||
| chr6:32843992-32844130 | Rare:31; Clinvar:1 | ||||
| chr6:32844384-32844848 | Common:1; Rare:104 | ||||
| chr6:32853660-32853778 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854010-32854234 | Common:2; Rare:55 | ||||
| chr6:32968454-32968616 | Common:3; Rare:43 | ||||
| chr6:32970865-32970946 | Common:1; Rare:29 | ||||
| chr6:32980118-32980358 | Common:1; Rare:75 | ||||
| chr6:33200356-33200449 | Rare:24 | ||||
| chr6:33200654-33200973 | Common:3; Rare:93 | ||||
| chr6:33202076-33202395 | Common:3; Rare:98 | ||||
| chr6:33208416-33208549 | Rare:33 | ||||
| chr6:33271823-33272140 | Common:2; Rare:126 | ||||
| chr6:33277125-33277176 | Rare:18 |