| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:49915452-49915818 | Common:4; Rare:113 | ||||
| chr20:50113106-50113244 | Common:5; Rare:69 | ||||
| chr20:50115935-50116092 | Common:2; Rare:36 | ||||
| chr20:50153651-50153903 | Common:2; Rare:99 | ||||
| chr20:50958490-50958874 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):3 | ||||
| chr20:53593793-53593902 | Common:1; Rare:41 | ||||
| chr20:56392182-56392692 | Common:6; Rare:134 | ||||
| chr20:57560974-57561237 | Rare:48; Clinvar:1 | ||||
| chr20:57563490-57563839 | Common:4; Rare:114; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr20:57710546-57710635 | Rare:22 | ||||
| chr20:58651080-58651305 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr20:58888788-58888841 | Rare:19 | ||||
| chr20:58892309-58892342 | Rare:10 | ||||
| chr20:59032219-59032578 | Common:3; Rare:153; Clinvar:1; Clinvar (benign):5 | ||||
| chr20:59042711-59043044 | Common:1; Rare:121 |