| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33206610-33207427 | Common:2; Rare:152 | ||||
| chr6:33207698-33207902 | Common:1; Rare:45 | ||||
| chr6:33212891-33213291 | Common:4; Rare:120 | ||||
| chr6:33248181-33248629 | Common:2; Rare:137 | ||||
| chr6:33249204-33249599 | Common:2; Rare:117 | ||||
| chr6:33425201-33425601 | Rare:53 | ||||
| chr6:33425620-33425817 | Common:2; Rare:49; Clinvar (benign):1 | ||||
| chr6:33425848-33426047 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:33426217-33426522 | Common:1; Rare:51 | ||||
| chr6:33426523-33426703 | Common:1; Rare:22 | ||||
| chr6:33426955-33427120 | Common:1; Rare:16 | ||||
| chr6:33571290-33571465 | Rare:39 | ||||
| chr6:33607370-33607680 | Common:2; Rare:53 | ||||
| chr6:33610931-33611097 | Rare:36 | ||||
| chr6:33745141-33745827 | Common:11; Rare:159 |