| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:56693227-56693465 | Rare:38 | ||||
| chr6:57046489-57046750 | Rare:90 | ||||
| chr6:57089883-57090232 | Rare:129 | ||||
| chr6:57172200-57172342 | Rare:42 | ||||
| chr6:57172515-57172764 | Common:1; Rare:79 | ||||
| chr6:57222276-57222364 | Rare:30 | ||||
| chr6:57317538-57317660 | Rare:36 | ||||
| chr6:63572152-63572748 | Rare:188 | ||||
| chr6:68634955-68635361 | Common:2; Rare:111 | ||||
| chr6:69796862-69797153 | Common:1; Rare:88; Clinvar:4; Clinvar (benign):3 | ||||
| chr6:70413188-70413577 | Common:2; Rare:114 | ||||
| chr6:70566851-70566998 | Common:2; Rare:59 | ||||
| chr6:70667713-70668021 | Common:4; Rare:119 | ||||
| chr6:73263144-73263224 | Common:2; Rare:21 | ||||
| chr6:73309876-73309925 | Rare:10 |