chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4183021820183021821CCAA16GENICheterozygous735238569
4183022663183022664GGA17GENIChomozygous735238570
4183024349183024350TC35GENIChomozygous612150319
4183024366183024367GA34GENIChomozygous612150320
4183024727183024728CCAAAA17GENICheterozygous735238572
4183026259183026260TTACAC12GENICpossibly homozygous735238574
4183026660183026661CT21GENIChomozygous612150321
4183027418183027420AA--15GENIChomozygous735238575
4183028012183028013TC27GENIChomozygous612150322
4183028022183028023GA31GENIChomozygous612150323
4183029418183029419GA29GENIChomozygous612150324
4183030153183030154GGTGA30GENIChomozygous735238577
4183030392183030393CT16GENIChomozygous612150325
4183030662183030663CT30GENIChomozygous612150326
4183030673183030674AG30GENIChomozygous612150327
4183032232183032233AC16GENIChomozygous612150328
4183032311183032312GT20GENIChomozygous612150329
4183032618183032619AG21GENIChomozygous612150330
4183033099183033103AAAA----12GENIChomozygous735238578
4183033102183033103AACC14GENICpossibly homozygous735238580
4183033554183033555CT32GENIChomozygous612150331
4183033565183033575CACACACACA----------8GENICheterozygous735238581
4183033622183033623AT18GENICheterozygous609534681
4183035208183035211AAA---13GENIChomozygous735238582
4183035223183035224AG16GENIChomozygous612150332
4183036184183036185TC21GENIChomozygous612150333
4183036319183036333GTGTGTGTGTGTGT--------------6GENIChomozygous735238584
4183036708183036709TC14GENIChomozygous612150334
4183037103183037104GT20GENIChomozygous609534682
4183037269183037270GA21GENIChomozygous612150335
4183037794183037795TC19GENIChomozygous612150336
4183037949183037950TG20GENIChomozygous609534683
4183038145183038146GA18GENIChomozygous612150337
4183039836183039837TA31GENIChomozygous609534684
4183040348183040349CT29GENIChomozygous612150338