chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18808525088085251CT6GENIChomozygous664426059
18808525388085254C-6GENIChomozygous765783431
18808525488085255GGCTCAGTGGTA5GENIChomozygous765783432
18808526188085262TTTGCCTG6GENIChomozygous765783433
18808528488085285GA8GENIChomozygous664426060
18808545888085459TA19GENIChomozygous664426061
18808831088088311AG19GENIChomozygous664426062
18808835088088351GGCACACA11GENIChomozygous765783436
18809022488090225TTTG17GENIChomozygous765783438
18809164588091646GA21GENIChomozygous664426063
18809171488091715GA19GENIChomozygous664426064
18809179488091795CG18GENIChomozygous664426065
18809216088092161GA24GENIChomozygous664426066
18809236388092364TTCA14GENIChomozygous765783439
18809254688092547TG27GENIChomozygous664426067
18809266988092670CT28GENIChomozygous664426068
18809287988092880AG21GENIChomozygous664426069
18809298788092988CG18GENIChomozygous664426070
18809314988093150GA23GENIChomozygous664426071
18809383888093839GA28GENIChomozygous664426072
18809410388094104TC33GENIChomozygous664426073
18809426288094263AG30GENIChomozygous664426074
18809426688094267TTCAATGAAGATCAGCATCAGCAAAGCC31GENIChomozygous765783440
18809457288094573GC29GENIChomozygous664426075
18809468888094689TC25GENIChomozygous664426076
18809476588094766GA26GENIChomozygous664426077
18809507188095072AG22GENIChomozygous664426078
18809622688096227GGGTGTGTGTGTGTGTGTGTGT10GENIChomozygous765783443
18809644188096442GA20GENIChomozygous664426079
18809652088096521TC24GENIChomozygous664426080
18809796988097970AG26GENIChomozygous664426081
18809803988098040TC22GENIChomozygous664426082
18809808688098087TC26GENIChomozygous664426083
18809869988098700GT20GENIChomozygous664426084
18809918888099189GGA21GENIChomozygous765783444
18809919688099197GGAA25GENIChomozygous765783446
18810002388100024CT27GENIChomozygous664426085