| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:69796877-69797146 | Common:1; Rare:79; Clinvar:4; Clinvar (benign):2 | ||||
| chr6:70566807-70566954 | Common:1; Rare:49 | ||||
| chr6:73521055-73521385 | Common:1; Rare:70 | ||||
| chr6:73521550-73521652 | Rare:26 | ||||
| chr6:73653919-73654130 | Common:2; Rare:52; Clinvar:3 | ||||
| chr6:73696110-73696229 | Rare:28 | ||||
| chr6:75205994-75206348 | Common:2; Rare:85 | ||||
| chr6:75284495-75285020 | Common:1; Rare:173 | ||||
| chr6:75493460-75493659 | Common:1; Rare:33 | ||||
| chr6:75493761-75493857 | Rare:22 | ||||
| chr6:75601730-75601883 | Common:1; Rare:50 | ||||
| chr6:75749058-75749349 | Common:4; Rare:93; Clinvar:3 | ||||
| chr6:78867477-78867605 | Rare:61 | ||||
| chr6:79234593-79234759 | Common:2; Rare:45 | ||||
| chr6:79537338-79537650 | Common:2; Rare:93; Clinvar:4 |