| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31665799-31666163 | Common:3; Rare:100 | ||||
| chr6:31703285-31703439 | Rare:51 | ||||
| chr6:31736260-31736585 | Common:2; Rare:81 | ||||
| chr6:31739771-31740042 | Common:2; Rare:70 | ||||
| chr6:31806774-31807095 | Common:4; Rare:130 | ||||
| chr6:31815320-31815556 | Common:1; Rare:72 | ||||
| chr6:31862773-31862875 | Common:1; Rare:40; Clinvar:3; Clinvar (benign):1 | ||||
| chr6:31897652-31897782 | Rare:26 | ||||
| chr6:31958897-31959191 | Rare:94; Clinvar:8 | ||||
| chr6:32153422-32153539 | Rare:19 | ||||
| chr6:32154380-32154448 | Rare:11 | ||||
| chr6:32177032-32177488 | Common:2; Rare:74 | ||||
| chr6:32178171-32178508 | Common:2; Rare:55 | ||||
| chr6:32190144-32190351 | Rare:39 | ||||
| chr6:32192864-32193145 | Common:1; Rare:39 |