| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56640037-56640239 | Rare:51; Clinvar:2; Clinvar (benign):3 | ||||
| chr6:57961351-57961674 | Common:2; Rare:96 | ||||
| chr6:73517829-73518266 | Common:2; Rare:117 | ||||
| chr6:79060484-79060724 | Rare:54 | ||||
| chr6:83124097-83124137 | Rare:4 | ||||
| chr6:83139838-83140110 | Common:2; Rare:55 | ||||
| chr6:85678708-85678969 | Rare:90 | ||||
| chr6:87700680-87700983 | Common:2; Rare:74 | ||||
| chr6:89083508-89083866 | Common:2; Rare:97 | ||||
| chr6:91066797-91067031 | Rare:50 | ||||
| chr6:93416711-93416958 | Common:1; Rare:64 | ||||
| chr6:105453412-105453660 | Common:1; Rare:41 | ||||
| chr6:106141679-106141949 | Rare:44 | ||||
| chr6:106220716-106220845 | Common:1; Rare:18 | ||||
| chr6:106561097-106561498 | Common:2; Rare:83 |