| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:39819804-39819965 | Common:3; Rare:37 | ||||
| chr6:44251449-44252075 | Common:2; Rare:218 | ||||
| chr6:44253187-44253515 | Common:3; Rare:114 | ||||
| chr6:53793668-53793774 | Common:1; Rare:18 | ||||
| chr6:57961347-57961648 | Common:2; Rare:93 | ||||
| chr6:71420816-71421005 | Common:1; Rare:61 | ||||
| chr6:73517858-73518266 | Common:2; Rare:108 | ||||
| chr6:85678712-85678952 | Rare:80 | ||||
| chr6:108589350-108589756 | Rare:85 | ||||
| chr6:108622769-108622934 | Common:1; Rare:29 | ||||
| chr6:111381370-111381613 | Common:1; Rare:45 | ||||
| chr6:111604159-111604384 | Rare:38 | ||||
| chr6:121437489-121437573 | Common:1; Rare:17 | ||||
| chr6:125790097-125790247 | Common:1; Rare:27 | ||||
| chr6:129505058-129505322 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 |