| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32167839-32167949 | Rare:23 | ||||
| chr6:32176056-32176228 | Common:1; Rare:36 | ||||
| chr6:32177047-32177261 | Rare:32 | ||||
| chr6:32589753-32590015 | Common:20; Rare:22 | ||||
| chr6:32637195-32637412 | Common:26; Rare:5 | ||||
| chr6:32838210-32838558 | Common:2; Rare:68; Clinvar (benign):1 | ||||
| chr6:32844009-32844115 | Rare:24; Clinvar:1 | ||||
| chr6:32844622-32844848 | Common:1; Rare:49 | ||||
| chr6:32853686-32853819 | Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:32854007-32854209 | Common:2; Rare:50 | ||||
| chr6:32970680-32970952 | Common:1; Rare:72 | ||||
| chr6:32976396-32976609 | Rare:81 | ||||
| chr6:33075713-33076035 | Common:6; Rare:42 | ||||
| chr6:33200639-33201125 | Common:3; Rare:116 | ||||
| chr6:33201814-33202125 | Common:4; Rare:82 |