| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73519881-73520214 | Common:1; Rare:120 | ||||
| chr6:73521183-73521492 | Common:1; Rare:67 | ||||
| chr6:73521547-73521625 | Rare:22 | ||||
| chr6:73653934-73654076 | Common:1; Rare:41; Clinvar:3 | ||||
| chr6:73695976-73696022 | Rare:5 | ||||
| chr6:73696044-73696275 | Rare:68 | ||||
| chr6:75284695-75285022 | Common:1; Rare:96 | ||||
| chr6:75601764-75601877 | Rare:39 | ||||
| chr6:75602279-75602530 | Common:1; Rare:72 | ||||
| chr6:75749069-75749303 | Common:3; Rare:79; Clinvar:3 | ||||
| chr6:78867456-78867615 | Rare:74 | ||||
| chr6:79078245-79078590 | Common:1; Rare:148 | ||||
| chr6:79537394-79537650 | Common:1; Rare:71; Clinvar:2 | ||||
| chr6:79947544-79947805 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:80004355-80004697 | Common:7; Rare:84 |