| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73653795-73654080 | Common:1; Rare:92; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr6:73695708-73696099 | Common:4; Rare:69 | ||||
| chr6:73696110-73696342 | Common:1; Rare:82 | ||||
| chr6:75284309-75284384 | Rare:24 | ||||
| chr6:75284589-75285070 | Common:1; Rare:159 | ||||
| chr6:75602374-75602572 | Common:1; Rare:61 | ||||
| chr6:75678675-75678886 | Rare:53 | ||||
| chr6:78867471-78867919 | Common:1; Rare:172 | ||||
| chr6:79078028-79078571 | Common:1; Rare:217 | ||||
| chr6:79234545-79234878 | Common:3; Rare:85 | ||||
| chr6:79537118-79537215 | Rare:26; Clinvar:1 | ||||
| chr6:79537428-79537588 | Rare:39 | ||||
| chr6:79947544-79947659 | Rare:49; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:80004378-80004705 | Common:6; Rare:80 | ||||
| chr6:82363473-82363902 | Common:4; Rare:125 |