Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:19233073-19233186 | Rare:35 | ||||
chr1:19270559-19270677 | Common:1; Rare:38 | ||||
chr1:19270788-19270810 | Common:1; Rare:5 | ||||
chr1:19273853-19274270 | Common:12; Rare:140 | ||||
chr1:19280185-19280337 | Rare:16 | ||||
chr1:19285912-19286376 | Common:3; Rare:163 | ||||
chr1:19287937-19288138 | Rare:50 | ||||
chr1:19410218-19410495 | Common:1; Rare:55 | ||||
chr1:19452278-19452470 | Rare:47 | ||||
chr1:20644236-20644540 | Common:1; Rare:78; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:20653745-20653866 | Rare:31; Clinvar:1 | ||||
chr1:20654294-20654704 | Common:4; Rare:130; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:20655679-20655976 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
chr1:21261975-21262088 | Common:2; Rare:22 | ||||
chr1:21617944-21618117 | Common:1; Rare:42 |