| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:28267070-28267156 | Common:2; Rare:17 | ||||
| chr6:30061155-30061327 | Rare:33 | ||||
| chr6:30571248-30571482 | Common:1; Rare:78 | ||||
| chr6:30742644-30742942 | Common:2; Rare:77 | ||||
| chr6:31665875-31666137 | Common:3; Rare:74 | ||||
| chr6:31958928-31959182 | Rare:69; Clinvar:5 | ||||
| chr6:33200656-33200923 | Common:2; Rare:82 | ||||
| chr6:33271980-33272126 | Common:1; Rare:79 | ||||
| chr6:33417885-33417940 | Rare:24 | ||||
| chr6:34757360-34757544 | Common:1; Rare:58 | ||||
| chr6:36678543-36678760 | Common:1; Rare:58 | ||||
| chr6:36874794-36874858 | Rare:26 | ||||
| chr6:42929210-42929494 | Common:3; Rare:74 | ||||
| chr6:43013908-43014290 | Common:1; Rare:80 | ||||
| chr6:43516887-43517112 | Common:4; Rare:85; Clinvar:2; Clinvar (benign):1 |