| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:16760768-16761105 | Common:4; Rare:85 | ||||
| chr6:16761390-16761568 | Common:1; Rare:49 | ||||
| chr6:17280809-17280992 | Common:2; Rare:58 | ||||
| chr6:17600189-17600401 | Common:5; Rare:79 | ||||
| chr6:17706791-17707003 | Common:1; Rare:63 | ||||
| chr6:18264383-18264790 | Common:1; Rare:164 | ||||
| chr6:18387218-18387510 | Common:2; Rare:91 | ||||
| chr6:20212397-20212739 | Common:2; Rare:92 | ||||
| chr6:20401545-20401857 | Common:3; Rare:80 | ||||
| chr6:24357484-24357609 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:24357627-24357722 | Rare:36; Clinvar:2 | ||||
| chr6:24357742-24358018 | Common:1; Rare:81 | ||||
| chr6:24358021-24358145 | Common:1; Rare:28 | ||||
| chr6:24402792-24403047 | Common:3; Rare:78 | ||||
| chr6:24666720-24666942 | Common:1; Rare:100 |