| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31897634-31897782 | Rare:34 | ||||
| chr6:31958899-31959191 | Rare:94; Clinvar:8 | ||||
| chr6:32128203-32128450 | Common:2; Rare:58 | ||||
| chr6:32151903-32152022 | Common:7; Rare:30 | ||||
| chr6:32154362-32154493 | Rare:16 | ||||
| chr6:32176041-32176219 | Common:1; Rare:39 | ||||
| chr6:32177331-32177385 | Rare:8 | ||||
| chr6:32844013-32844115 | Rare:22; Clinvar:1 | ||||
| chr6:32844634-32844822 | Common:1; Rare:39 | ||||
| chr6:32853705-32853783 | Rare:36; Clinvar (benign):1 | ||||
| chr6:32853985-32854209 | Common:2; Rare:52 | ||||
| chr6:32968480-32968621 | Common:2; Rare:41 | ||||
| chr6:32968825-32968933 | Common:2; Rare:31 | ||||
| chr6:32976396-32976707 | Rare:128 | ||||
| chr6:33200352-33200443 | Rare:24 |