Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:63520632-63520849 | Common:3; Rare:105 | ||||
chr20:63574211-63574346 | Common:1; Rare:32 | ||||
chr20:63658230-63658329 | Common:4; Rare:27 | ||||
chr20:63707866-63708057 | Rare:52 | ||||
chr20:63865089-63865351 | Common:2; Rare:102 | ||||
chr20:64079924-64080111 | Common:2; Rare:79 | ||||
chr20:64255629-64255776 | Common:3; Rare:79 | ||||
chr21:25607457-25607564 | Rare:60 | ||||
chr21:25639574-25639746 | Rare:29 | ||||
chr21:25734858-25734972 | Common:2; Rare:49 | ||||
chr21:25735001-25735382 | Common:1; Rare:119 | ||||
chr21:26170617-26170874 | Common:3; Rare:89; Clinvar:5; Clinvar (benign):2 | ||||
chr21:28992827-28993119 | Common:2; Rare:119 | ||||
chr21:29073555-29073870 | Common:2; Rare:98 | ||||
chr21:31659487-31659837 | Common:2; Rare:156; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |