| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31827546-31827938 | Common:8; Rare:177 | ||||
| chr6:31834614-31834946 | Common:4; Rare:77 | ||||
| chr6:31870935-31871252 | Common:1; Rare:57 | ||||
| chr6:31877650-31877998 | Rare:49 | ||||
| chr6:31878955-31879107 | Common:2; Rare:38 | ||||
| chr6:31897670-31897782 | Rare:21 | ||||
| chr6:31945774-31946157 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr6:31949219-31949530 | Common:1; Rare:82; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:31950142-31950397 | Common:1; Rare:77; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:31958902-31959373 | Rare:159; Clinvar:8 | ||||
| chr6:32109282-32109493 | Rare:34 | ||||
| chr6:32117673-32117977 | Common:2; Rare:71 | ||||
| chr6:32154376-32154487 | Rare:14 | ||||
| chr6:32154764-32155072 | Rare:64 | ||||
| chr6:32176056-32176210 | Rare:31 |