| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:25195606-25196001 | Common:10; Rare:111 | ||||
| chr20:25221743-25221906 | Common:1; Rare:36 | ||||
| chr20:25223295-25223565 | Common:1; Rare:45 | ||||
| chr20:25247961-25248392 | Common:2; Rare:175 | ||||
| chr20:25390519-25390674 | Rare:71; Clinvar:1 | ||||
| chr20:25390817-25390992 | Common:1; Rare:53; Clinvar:2; Clinvar (benign):1 | ||||
| chr20:25623938-25624188 | Common:1; Rare:99 | ||||
| chr20:25696744-25697053 | Common:3; Rare:90 | ||||
| chr20:31514697-31514731 | Rare:9 | ||||
| chr20:31545258-31545466 | Common:1; Rare:32 | ||||
| chr20:31547233-31547504 | Common:1; Rare:77 | ||||
| chr20:31547690-31547750 | Rare:13 | ||||
| chr20:31566205-31566391 | Rare:50 | ||||
| chr20:31605109-31605374 | Common:8; Rare:130 | ||||
| chr20:31722439-31722937 | Common:1; Rare:110 |