chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18808525088085251CT6GENIChomozygous62139535
18808525388085254C-6GENIChomozygous62139536
18808525488085255GGCTCAGTGGTA5GENIChomozygous62139537
18808526188085262TTTGCCTG6GENIChomozygous60758308
18808528488085285GA8GENIChomozygous62015492
18808545888085459TA19GENIChomozygous62015493
18808831088088311AG19GENIChomozygous61458039
18808835088088351GGCACACA11GENIChomozygous62015494
18809022488090225TTTG17GENIChomozygous61458048
18809171488091715GA19GENIChomozygous61458049
18809179488091795CG18GENIChomozygous61458050
18809216088092161GA24GENIChomozygous62262679
18809236388092364TTCA14GENIChomozygous61458051
18809254688092547TG27GENIChomozygous61458052
18809266988092670CT28GENIChomozygous61458053
18809287988092880AG21GENIChomozygous61458054
18809298788092988CG18GENIChomozygous61458055
18809314988093150GA23GENIChomozygous62262680
18809383888093839GA28GENIChomozygous62262681
18809410388094104TC33GENIChomozygous61458057
18809426288094263AG30GENIChomozygous61458058
18809426688094267TTCAATGAAGATCAGCATCAGCAAAGCC31GENIChomozygous61458059
18809457288094573GC29GENIChomozygous61458061
18809468888094689TC25GENIChomozygous61458064
18809476588094766GA26GENIChomozygous62262682
18809507188095072AG22GENIChomozygous61458066
18809622688096227GGGTGTGTGTGTGTGTGTGTGT10GENIChomozygous62139539
18809796988097970AG26GENIChomozygous62015498
18809803988098040TC22GENIChomozygous62015499
18809808688098087TC26GENIChomozygous61458071
18809918888099189GGA21GENIChomozygous62569160
18809164588091646GA21GENIChomozygous62569156
18809644188096442GA20GENIChomozygous62569157
18809652088096521TC24GENIChomozygous62569158
18809869988098700GT20GENIChomozygous62569159
18809919688099197GGAA25GENIChomozygous62311289
18810002388100024CT27GENIChomozygous62569162