| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:48921588-48921916 | Common:3; Rare:133; Clinvar:4; Clinvar (benign):4 | ||||
| chr20:49046147-49046408 | Common:3; Rare:81 | ||||
| chr20:49046665-49046873 | Common:3; Rare:72 | ||||
| chr20:49219211-49219541 | Common:1; Rare:138 | ||||
| chr20:49278031-49278291 | Rare:71 | ||||
| chr20:49812772-49812925 | Common:2; Rare:43 | ||||
| chr20:49915471-49915602 | Common:3; Rare:49 | ||||
| chr20:49936278-49936429 | Rare:63 | ||||
| chr20:50113106-50113280 | Common:6; Rare:80 | ||||
| chr20:50115932-50116061 | Common:1; Rare:30 | ||||
| chr20:50153633-50153939 | Common:2; Rare:124 | ||||
| chr20:50190540-50190833 | Rare:86 | ||||
| chr20:50510076-50510446 | Common:3; Rare:145 | ||||
| chr20:50794854-50795099 | Common:1; Rare:90 | ||||
| chr20:50930859-50931011 | Rare:51 |