| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:73394619-73394900 | Common:4; Rare:89 | ||||
| chr6:73520973-73521414 | Common:4; Rare:120 | ||||
| chr6:73521555-73521619 | Rare:17 | ||||
| chr6:73653903-73654162 | Common:3; Rare:69; Clinvar:3 | ||||
| chr6:75205782-75206085 | Common:1; Rare:80 | ||||
| chr6:75206089-75206282 | Common:1; Rare:47 | ||||
| chr6:75284695-75285033 | Common:1; Rare:101 | ||||
| chr6:75601766-75601904 | Rare:51 | ||||
| chr6:75749080-75749308 | Common:3; Rare:74; Clinvar:3 | ||||
| chr6:78867470-78867615 | Rare:71 | ||||
| chr6:79234556-79234771 | Common:2; Rare:55 | ||||
| chr6:79537124-79537222 | Rare:26; Clinvar:1 | ||||
| chr6:79537302-79537676 | Common:3; Rare:119; Clinvar:5 | ||||
| chr6:79631173-79631374 | Common:2; Rare:48 | ||||
| chr6:80106407-80106705 | Common:2; Rare:100; Clinvar (pathogenic):1 |