| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:32119092-32119294 | Rare:45 | ||||
| chr6:32180784-32181003 | Common:1; Rare:31 | ||||
| chr6:32215455-32215750 | Rare:38 | ||||
| chr6:32442234-32442693 | Common:6; Rare:104 | ||||
| chr6:32894153-32894314 | Common:1; Rare:31 | ||||
| chr6:32894581-32894958 | Common:14; Rare:117 | ||||
| chr6:32980455-32980721 | Common:8; Rare:123 | ||||
| chr6:33346033-33346073 | Common:1; Rare:8 | ||||
| chr6:33425657-33425872 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:33658382-33658709 | Common:1; Rare:73 | ||||
| chr6:33684015-33684390 | Common:2; Rare:104 | ||||
| chr6:33684416-33684688 | Rare:87 | ||||
| chr6:33685218-33685396 | Common:2; Rare:44 | ||||
| chr6:33685640-33686253 | Common:3; Rare:167 | ||||
| chr6:33686858-33687564 | Common:2; Rare:202 |