| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73696019-73696218 | Common:1; Rare:41 | ||||
| chr6:75152130-75152350 | Common:1; Rare:60; Clinvar:3; Clinvar (benign):2 | ||||
| chr6:75205229-75205392 | Common:1; Rare:24 | ||||
| chr6:75205782-75206300 | Common:2; Rare:130 | ||||
| chr6:75284553-75284565 | Rare:2 | ||||
| chr6:75284671-75285028 | Common:1; Rare:107 | ||||
| chr6:75493476-75493866 | Common:1; Rare:74 | ||||
| chr6:75493879-75493926 | Common:1; Rare:10 | ||||
| chr6:75601771-75601924 | Rare:59 | ||||
| chr6:75602370-75602534 | Common:1; Rare:43 | ||||
| chr6:78867470-78867600 | Rare:59 | ||||
| chr6:79234553-79234764 | Common:2; Rare:57 | ||||
| chr6:79537153-79537228 | Rare:18; Clinvar:1 | ||||
| chr6:79537289-79537688 | Common:3; Rare:129; Clinvar:5 | ||||
| chr6:79631201-79631378 | Common:1; Rare:47 |