| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31652123-31652463 | Common:9; Rare:92 | ||||
| chr6:31665196-31665440 | Common:1; Rare:65 | ||||
| chr6:31665574-31666146 | Common:7; Rare:149 | ||||
| chr6:31703297-31703439 | Rare:45 | ||||
| chr6:31730143-31730583 | Common:3; Rare:108 | ||||
| chr6:31736259-31736610 | Common:2; Rare:87 | ||||
| chr6:31753369-31753634 | Rare:82 | ||||
| chr6:31763937-31764250 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr6:31777304-31777529 | Common:2; Rare:39 | ||||
| chr6:31795631-31795986 | Common:1; Rare:76 | ||||
| chr6:31806681-31807003 | Rare:131 | ||||
| chr6:31815312-31815576 | Common:1; Rare:92 | ||||
| chr6:31827883-31827936 | Common:2; Rare:32 | ||||
| chr6:31834849-31835087 | Common:5; Rare:98 | ||||
| chr6:31837321-31837470 | Common:1; Rare:58 |