| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:44210745-44210980 | Common:3; Rare:82 | ||||
| chr20:44885439-44885798 | Common:6; Rare:114 | ||||
| chr20:44909953-44910105 | Common:2; Rare:59 | ||||
| chr20:44960370-44960564 | Common:1; Rare:68 | ||||
| chr20:44966391-44966531 | Rare:49 | ||||
| chr20:45857357-45857602 | Common:3; Rare:60 | ||||
| chr20:45891256-45891360 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:47501752-47501937 | Common:1; Rare:66 | ||||
| chr20:49046166-49046358 | Common:3; Rare:57 | ||||
| chr20:49278037-49278369 | Common:2; Rare:88 | ||||
| chr20:49936255-49936407 | Rare:61 | ||||
| chr20:50113112-50113293 | Common:6; Rare:79 | ||||
| chr20:50958519-50958834 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr20:56392182-56392454 | Common:1; Rare:80 |