| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:42746074-42746358 | Rare:75 | ||||
| chr6:42879577-42879952 | Rare:113 | ||||
| chr6:42890789-42890923 | Rare:52 | ||||
| chr6:42929097-42929202 | Rare:29 | ||||
| chr6:42929204-42929571 | Common:4; Rare:109 | ||||
| chr6:42929679-42929844 | Common:1; Rare:58 | ||||
| chr6:42984297-42984600 | Rare:72 | ||||
| chr6:43013831-43014321 | Common:2; Rare:122 | ||||
| chr6:43053774-43054017 | Common:2; Rare:77; Clinvar:5; Clinvar (benign):1 | ||||
| chr6:43059822-43059948 | Common:1; Rare:39 | ||||
| chr6:43060247-43060549 | Common:1; Rare:84 | ||||
| chr6:43171332-43171516 | Rare:60 | ||||
| chr6:43182104-43182228 | Rare:36 | ||||
| chr6:43229328-43229515 | Rare:66 | ||||
| chr6:43516800-43517141 | Common:5; Rare:128; Clinvar:2; Clinvar (benign):1 |