| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31665790-31666166 | Common:3; Rare:104 | ||||
| chr6:31703285-31703439 | Rare:51 | ||||
| chr6:31736473-31736623 | Common:1; Rare:34 | ||||
| chr6:31739732-31740020 | Common:3; Rare:68 | ||||
| chr6:31806672-31807072 | Common:3; Rare:165 | ||||
| chr6:31827275-31827313 | Rare:9 | ||||
| chr6:31834538-31834937 | Common:3; Rare:110 | ||||
| chr6:31862782-31862875 | Common:1; Rare:34; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31897651-31897782 | Rare:26 | ||||
| chr6:31958897-31959338 | Rare:154; Clinvar:8 | ||||
| chr6:32127750-32127896 | Rare:39 | ||||
| chr6:32130179-32130395 | Common:2; Rare:39 | ||||
| chr6:32153403-32153564 | Rare:26 | ||||
| chr6:32153753-32154216 | Common:4; Rare:78 | ||||
| chr6:32154749-32155053 | Rare:60 |