| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47501758-47501993 | Common:1; Rare:80 | ||||
| chr20:48921577-48921934 | Common:3; Rare:142; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:49046160-49046358 | Common:3; Rare:59 | ||||
| chr20:49219234-49219518 | Common:1; Rare:125 | ||||
| chr20:49278020-49278288 | Rare:72 | ||||
| chr20:49812807-49812926 | Common:1; Rare:30 | ||||
| chr20:49915479-49915574 | Common:2; Rare:36 | ||||
| chr20:49936255-49936423 | Rare:68 | ||||
| chr20:50113112-50113268 | Common:6; Rare:72 | ||||
| chr20:50115926-50116087 | Common:2; Rare:38 | ||||
| chr20:50153656-50153928 | Common:2; Rare:111 | ||||
| chr20:50510076-50510471 | Common:3; Rare:153 | ||||
| chr20:50930840-50931023 | Rare:63 | ||||
| chr20:50958471-50958857 | Common:1; Rare:140; Clinvar:1; Clinvar (benign):4 | ||||
| chr20:51562787-51563064 | Common:3; Rare:56 |