| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31736261-31736610 | Common:2; Rare:86 | ||||
| chr6:31897676-31897787 | Rare:21 | ||||
| chr6:31958850-31959182 | Rare:100; Clinvar:8 | ||||
| chr6:32154315-32154487 | Rare:24 | ||||
| chr6:32176027-32176254 | Common:1; Rare:47 | ||||
| chr6:32178102-32178468 | Common:2; Rare:56 | ||||
| chr6:32843876-32844123 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:32854024-32854216 | Common:2; Rare:49 | ||||
| chr6:32968391-32968667 | Common:5; Rare:81 | ||||
| chr6:33200656-33200948 | Common:2; Rare:89 | ||||
| chr6:33208630-33208769 | Common:3; Rare:34 | ||||
| chr6:33271646-33272150 | Common:3; Rare:179 | ||||
| chr6:33289169-33289644 | Common:4; Rare:111 | ||||
| chr6:33418048-33418454 | Common:2; Rare:96 | ||||
| chr6:33580158-33580369 | Common:2; Rare:57 |