Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:45791853-45792014 | Common:1; Rare:61 | ||||
chr20:45857357-45857617 | Common:3; Rare:63 | ||||
chr20:45891174-45891353 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1 | ||||
chr20:49219281-49219443 | Rare:83 | ||||
chr20:49278039-49278269 | Rare:64 | ||||
chr20:50113127-50113244 | Common:5; Rare:59 | ||||
chr20:50958497-50958830 | Common:1; Rare:105; Clinvar:1; Clinvar (benign):3 | ||||
chr20:62386985-62387115 | Common:3; Rare:52 | ||||
chr20:63707898-63708071 | Rare:48 | ||||
chr21:25607470-25607584 | Rare:57 | ||||
chr21:25734859-25735082 | Common:2; Rare:97 | ||||
chr21:32392986-32393163 | Common:2; Rare:73 | ||||
chr21:32612557-32612895 | Rare:84 | ||||
chr21:33542832-33543081 | Common:2; Rare:86 | ||||
chr21:37073077-37073348 | Common:4; Rare:110 |