chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65449127354491274T74GENIChomozygous128341609
65449128854491289T73GENIChomozygous128341610
65449945554499456AC66GENICheterozygous115059878
65451953354519533AAATGG29GENIChomozygous128341624
65453805954538059TGCTTGCT27GENIChomozygous128341637
65454936254549363TC39GENIChomozygous114804470
65454936954549370G37GENIChomozygous128341638
65454944454549445C24GENIChomozygous128341639
65458567054585671GC14GENIChomozygous114804521
65458568254585683AC12GENIChomozygous114804522
65458572554585726AC14GENIChomozygous118627905
65458572954585730GC16GENIChomozygous118627906
65458573454585735GT18GENIChomozygous118627907
65458573554585736AT19GENIChomozygous118627908
65458573754585738AC20GENIChomozygous118627909
65458573854585739AT20GENIChomozygous118627910
65458573954585740GT20GENIChomozygous118627911
65458574554585746CT19GENIChomozygous118627912
65458574954585750CT19GENIChomozygous118627913
65458576054585761AC19GENIChomozygous118627914
65458576154585762GT19GENIChomozygous118627915
65456963354569778CTCCCTCCCTCCCTCCCTTTGGACCGGCGGCCGGCTGGGGGGGCGGTTCCTCTTAAGGTCTGCAGCAGGAATGGGGCGGGGGGTAGAGAGAATGGGTGTGAGACGGCAAGAAGGAAGGAAGGGGGGAGCGGGCGGAGGACGGACG18GENIChomozygous130556383
65458575254585753AC18GENIChomozygous130334213
65458575354585754GT19GENIChomozygous130334214
65458575754585758AT20GENIChomozygous130334215
65458576554585767AG19GENIChomozygous130326755
65458576854585771AAG19GENIChomozygous130326756
65458577554585777AG19GENIChomozygous130326757