| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44251094-44251393 | Common:2; Rare:90 | ||||
| chr6:47606210-47606640 | Common:1; Rare:109; Clinvar (benign):1 | ||||
| chr6:50133852-50133953 | Common:1; Rare:18 | ||||
| chr6:52420876-52421025 | Rare:30 | ||||
| chr6:52505918-52506078 | Common:1; Rare:47 | ||||
| chr6:52535810-52535871 | Rare:9 | ||||
| chr6:52539707-52539810 | Common:1; Rare:22 | ||||
| chr6:52566859-52567223 | Common:8; Rare:59 | ||||
| chr6:52595342-52595567 | Common:1; Rare:30 | ||||
| chr6:52668603-52668834 | Common:2; Rare:36 | ||||
| chr6:53347987-53348026 | Rare:8 | ||||
| chr6:53519411-53519566 | Common:1; Rare:27 | ||||
| chr6:53793668-53793817 | Common:2; Rare:25 | ||||
| chr6:56579632-56579677 | Common:1; Rare:10 | ||||
| chr6:56580461-56580753 | Common:3; Rare:56 |