Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:188994571-188994805 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
chr2:188996176-188996405 | Common:12; Rare:50; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr2:207239367-207239684 | Rare:49 | ||||
chr2:237434804-237435031 | Common:2; Rare:40 | ||||
chr20:3784991-3785083 | Common:1; Rare:26 | ||||
chr20:19974494-19974793 | Rare:90; Clinvar (benign):4 | ||||
chr20:36050349-36050729 | Common:1; Rare:138 | ||||
chr20:53592747-53592772 | Rare:6 | ||||
chr21:16194265-16194607 | Common:2; Rare:94 | ||||
chr21:16588577-16588620 | Rare:8 | ||||
chr21:26844481-26844577 | Rare:36 | ||||
chr21:34887996-34888022 | Rare:3 | ||||
chr21:45992185-45992390 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):3 | ||||
chr21:46117112-46117446 | Common:3; Rare:98; Clinvar:3; Clinvar (benign):1 | ||||
chr22:22298078-22298210 | Common:2; Rare:47 |