| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31958891-31959191 | Rare:97; Clinvar:8 | ||||
| chr6:32038238-32038418 | Common:1; Rare:45 | ||||
| chr6:32109224-32109395 | Rare:34 | ||||
| chr6:32153757-32154227 | Common:4; Rare:79 | ||||
| chr6:32154363-32154487 | Rare:15 | ||||
| chr6:32177038-32177182 | Rare:25 | ||||
| chr6:32177331-32177371 | Rare:7 | ||||
| chr6:32178085-32178512 | Common:3; Rare:74 | ||||
| chr6:32190131-32190330 | Rare:42 | ||||
| chr6:32843992-32844136 | Rare:33; Clinvar:1 | ||||
| chr6:32844328-32844414 | Rare:20 | ||||
| chr6:32844631-32844848 | Common:1; Rare:48 | ||||
| chr6:32853680-32853777 | Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:32853989-32854216 | Common:2; Rare:52 | ||||
| chr6:32968497-32968621 | Common:1; Rare:35 |