| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32955133-32955208 | Rare:9 | ||||
| chr6:33014853-33015073 | Common:1; Rare:38 | ||||
| chr6:33019124-33019133 | Rare:1 | ||||
| chr6:33019283-33019599 | Common:9; Rare:43 | ||||
| chr6:33027664-33027716 | Common:3; Rare:6 | ||||
| chr6:33029445-33029597 | Rare:25 | ||||
| chr6:33029921-33030111 | Common:3; Rare:28 | ||||
| chr6:33075276-33075417 | Common:2; Rare:23 | ||||
| chr6:33161512-33161657 | Common:1; Rare:34 | ||||
| chr6:33170247-33170432 | Common:1; Rare:48; Clinvar (benign):3 | ||||
| chr6:33248378-33248515 | Rare:28 | ||||
| chr6:33249104-33249666 | Common:2; Rare:158 | ||||
| chr6:33392616-33392643 | Rare:2 | ||||
| chr6:33416411-33416607 | Common:1; Rare:51 | ||||
| chr6:33425224-33425323 | Rare:15 |