| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32970160-32970418 | Common:5; Rare:62 | ||||
| chr6:32970739-32970964 | Common:1; Rare:61 | ||||
| chr6:32976396-32976728 | Rare:133 | ||||
| chr6:32977531-32978004 | Common:4; Rare:169; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:33009554-33009787 | Common:3; Rare:49 | ||||
| chr6:33075761-33076046 | Common:4; Rare:38 | ||||
| chr6:33200334-33200432 | Rare:27 | ||||
| chr6:33200637-33200976 | Common:3; Rare:97 | ||||
| chr6:33208443-33208810 | Common:3; Rare:103 | ||||
| chr6:33271644-33272122 | Common:3; Rare:171 | ||||
| chr6:33277552-33277621 | Rare:19 | ||||
| chr6:33288953-33289061 | Rare:42 | ||||
| chr6:33289169-33289644 | Common:4; Rare:111 | ||||
| chr6:33296442-33296695 | Common:1; Rare:67 | ||||
| chr6:33298608-33299071 | Common:1; Rare:84 |