chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4145559509145559510AG30GENIChomozygous112871121
4145559644145559645AG35GENIChomozygous112871122
4145559940145559941CG28GENIChomozygous112871123
4145560219145560220AC34GENIChomozygous112871124
4145561219145561220TC23GENIChomozygous112871125
4145561295145561296TC21GENIChomozygous112871126
4145561681145561682CA37GENIChomozygous112871127
4145562627145562628CT26GENIChomozygous112871136
4145562811145562812GA24GENIChomozygous112871137
4145562883145562884AG22GENIChomozygous112871138
4145562980145562981TC24GENIChomozygous112871139
4145563235145563236CT17GENIChomozygous112871140
4145563691145563692GT38GENIChomozygous113179048
4145563906145563907CT26GENIChomozygous112871141
4145564300145564301TG23GENIChomozygous112871142
4145564646145564647AG19GENIChomozygous112871143
4145564814145564815AT21GENIChomozygous112871144
4145564961145564962CT16GENIChomozygous112871145
4145565283145565284CA30GENIChomozygous112871146
4145565616145565617TA28GENIChomozygous112871150
4145566736145566737CT25GENIChomozygous112871156
4145567107145567108CT25GENIChomozygous112871157
4145568828145568829GA19GENIChomozygous112871163
4145569084145569085CG32GENIChomozygous112871164
4145570239145570240TC35GENIChomozygous112871165
4145570481145570482CG23GENIChomozygous112871166
4145571600145571601AT20GENICpossibly homozygous113179050
4145571832145571833TC32GENIChomozygous112871168
4145572363145572364GA28GENIChomozygous112871169
4145572611145572612TC32GENIChomozygous112871170
4145573520145573521TC24GENIChomozygous112871171
4145574270145574271TA31GENIChomozygous112871172