chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46170732961707330GA6INTERGENIChomozygous56917071
46170807361708074GGC23INTERGENIChomozygous56917073
46170832061708321TTC33INTERGENIChomozygous56917074
46170892761708931TCTC----14INTERGENIChomozygous56917075
46170932661709327AC41INTERGENIChomozygous56917077
46171224561712246CT28INTERGENIChomozygous56917079
46171257761712578GC27INTERGENIChomozygous56917080
46171266661712667AG12INTERGENIChomozygous56917081
46171288261712883GGGT11INTERGENIChomozygous56917082
46170807561708076GC23INTERGENIChomozygous58508785
46170810961708110TTTTTCCTGAGAGGTTTGAGGCAAGACTGCTCTGGTTGTTAGGTTTTTTTGTTTGTTTGTTTGTTTGTTTGCTTG17INTERGENIChomozygous58336556
46171015961710160TTTCTC10INTERGENIChomozygous58336557
46171308261713083GA68INTERGENIChomozygous56917083
46171372361713724CT27INTERGENIChomozygous56917084
46171396961713970TC27INTERGENICpossibly homozygous56917085
46171427161714272GA17INTERGENIChomozygous56917086
46171447361714474G-17INTERGENIChomozygous56917087
46171453961714541AC--10INTERGENIChomozygous56917088
46171483261714833TA6INTERGENIChomozygous57329894
46171750161717502CT17INTERGENIChomozygous56917093
46171904561719046AG57INTERGENIChomozygous56917094