| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149718046-149718187 | Common:2; Rare:51 | ||||
| chr6:149749584-149749785 | Rare:101 | ||||
| chr6:150866330-150866537 | Rare:82 | ||||
| chr6:151240234-151240421 | Common:1; Rare:49 | ||||
| chr6:151325322-151325780 | Common:2; Rare:100 | ||||
| chr6:151391516-151391756 | Common:3; Rare:56 | ||||
| chr6:151452022-151452552 | Common:5; Rare:189; Clinvar (benign):3 | ||||
| chr6:151493996-151494137 | Common:1; Rare:43 | ||||
| chr6:152302001-152302198 | Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152636157-152636304 | Common:1; Rare:31 | ||||
| chr6:152636728-152637013 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152637227-152637294 | Rare:18 | ||||
| chr6:152983555-152983743 | Common:3; Rare:73 | ||||
| chr6:153002643-153002861 | Common:4; Rare:78 | ||||
| chr6:154510567-154510802 | Common:2; Rare:74 |