chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
125018722150187222CT15GENICpossibly homozygous50236814
125018749150187492TC10GENIChomozygous50236816
125018749350187494CT11GENIChomozygous50343969
125018776750187768AG3GENICheterozygous50513876
125018778750187788TTCAGGACA1GENIChomozygous50236822
125018881850188819CA12GENIChomozygous50236832
125018898050188981GC21GENIChomozygous50236834
125019034050190341TC25GENIChomozygous50236836
125019048250190483GA23GENIChomozygous50236838
125019131650191317GA12GENICpossibly homozygous50236840
125019134250191343T-8GENIChomozygous50236842
125019139350191394GT14GENICpossibly homozygous50236844
125019157650191577CCA2GENICheterozygous50236848
125019166650191667GA22GENICpossibly homozygous50236850
125019188750191888G-1GENIChomozygous50236854
125019211250192113TC13GENIChomozygous50236856
125019591350195914GA4GENIChomozygous50236866
125019611450196115AG13GENICheterozygous50236868
125019622050196221AG26GENICpossibly homozygous50236870
125019816650198167TC30GENIChomozygous50236872
125019845350198454G-2GENICheterozygous50236874
125019865050198651G-6GENIChomozygous50236876
125021218750212188GT3GENIChomozygous50236890
125021331650213322GTGTGT------1GENIChomozygous50546848
125021513050215131TC5GENIChomozygous50236900
125021513350215134TC5GENIChomozygous50236901
125021535250215353GA19GENIChomozygous50236907
125021642150216422GA5GENICheterozygous50236911
125021995150219952AG18GENIChomozygous50236919
125022097050220971AG14GENICpossibly homozygous50236921
125022304450223045AG14GENIChomozygous50236923
125022755550227556GGC14GENIChomozygous50236931
125022759450227595AG9GENICpossibly homozygous50236933
125022788850227889CT10GENIChomozygous50236935
125022920750229208AG18GENICpossibly homozygous50236937