Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:44210751-44211061 | Common:5; Rare:112 | ||||
chr20:45857357-45857598 | Common:3; Rare:59 | ||||
chr20:45891237-45891400 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
chr20:45934627-45934705 | Rare:44 | ||||
chr20:47356678-47356919 | Rare:59 | ||||
chr20:49278019-49278269 | Rare:66 | ||||
chr20:50113131-50113244 | Common:5; Rare:56 | ||||
chr20:50958496-50958818 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
chr20:54173979-54174120 | Rare:45 | ||||
chr20:56392187-56392389 | Rare:50 | ||||
chr20:56468423-56468700 | Rare:101 | ||||
chr20:58515390-58515521 | Common:2; Rare:23 | ||||
chr20:59032269-59032573 | Common:3; Rare:127; Clinvar (benign):4 | ||||
chr20:62386968-62387126 | Common:3; Rare:67 | ||||
chr20:62937883-62938189 | Common:2; Rare:111 |