chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14782943947829440GA17GENIChomozygous141206793
14782955547829556TC28GENIChomozygous141206794
14782972047829721AG24GENIChomozygous141206795
14782984847829849AG19GENIChomozygous141206796
14782987447829875TC16GENIChomozygous141206797
14783012247830123GA21GENIChomozygous141206798
14783044747830448AG25GENIChomozygous141206799
14783104547831046CT18GENIChomozygous141206800
14783107947831080AG18GENIChomozygous141206801
14783112447831125CG13GENIChomozygous141206802
14783149947831500CT17GENIChomozygous141206803
14783162447831624AG29GENIChomozygous141160768
14783235247832354AA19GENIChomozygous141160769
14783238247832386TATA14GENIChomozygous141160770
14783239147832392A16GENIChomozygous403538620
14783235247832353AT19GENICheterozygous153826327
14783235247832353A19GENIChomozygous403538619
14783239147832392AG16GENICheterozygous153826328
14783239947832400A16GENIChomozygous403538621
14783239947832400AG16GENICheterozygous403538622
14783240147832402A16GENIChomozygous403538623
14783240147832402AG16GENICheterozygous403538624
14783240247832403T16GENIChomozygous403538625
14783240247832403TC16GENICheterozygous403538626
14783311347833114TC22GENIChomozygous141206804
14783339547833396GT25GENIChomozygous141206805
14783394447833945GA22GENIChomozygous141206809
14783350047833501AG27GENIChomozygous141206806
14783353647833537GC27GENIChomozygous141206807
14783383347833834AT24GENIChomozygous141206808
14783403547834041TTAACG21GENIChomozygous141160771
14783413947834140AT19GENIChomozygous141206810
14783421447834215CT23GENIChomozygous141206811
14783426747834272CTTCA29GENIChomozygous141160772
14783502847835029TC16GENIChomozygous141206812
14783525547835256T15GENIChomozygous141160773
14783616447836165AG17GENIChomozygous141206813
14783651447836515CT16GENIChomozygous141206814
14783657247836573CG13GENIChomozygous141206815
14783599047835991AC11GENIChomozygous145259197