| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31729264-31729373 | Rare:16 | ||||
| chr6:31739751-31740021 | Common:2; Rare:63 | ||||
| chr6:31815285-31815550 | Common:1; Rare:79 | ||||
| chr6:31827275-31827329 | Rare:10 | ||||
| chr6:31827481-31827790 | Common:5; Rare:111 | ||||
| chr6:31834660-31834924 | Common:3; Rare:55 | ||||
| chr6:31897673-31897782 | Rare:20 | ||||
| chr6:31933610-31933964 | Rare:114 | ||||
| chr6:31943930-31944212 | Common:1; Rare:77; Clinvar (benign):2 | ||||
| chr6:31947717-31948081 | Common:3; Rare:95; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr6:31950602-31950944 | Common:3; Rare:101; Clinvar (benign):3 | ||||
| chr6:31951132-31951473 | Common:1; Rare:90; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr6:31958881-31959363 | Rare:164; Clinvar:8 | ||||
| chr6:31996012-31996323 | Rare:85 | ||||
| chr6:32128186-32128422 | Common:2; Rare:59 |