Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367728-169368294 | Common:4; Rare:120 | ||||
chr1:169485925-169486142 | Rare:54; Clinvar:2 | ||||
chr1:169794890-169795053 | Common:3; Rare:34 | ||||
chr1:171485329-171485555 | Rare:75 | ||||
chr1:173477127-173477492 | Common:4; Rare:136 | ||||
chr1:173824331-173824732 | Rare:79; Clinvar:2 | ||||
chr1:179882488-179882852 | Rare:173; Clinvar:7; Clinvar (benign):2 | ||||
chr1:182839030-182839351 | Common:2; Rare:100 | ||||
chr1:183635644-183636095 | Common:4; Rare:126 | ||||
chr1:185156897-185157294 | Common:2; Rare:108 | ||||
chr1:186375681-186375899 | Common:1; Rare:58 | ||||
chr1:193059309-193059665 | Rare:165 | ||||
chr1:201946473-201946685 | Common:2; Rare:31 | ||||
chr1:202010391-202010587 | Common:1; Rare:44 | ||||
chr1:204516344-204516483 | Common:1; Rare:52 |