chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120572113120572114GT24GENIChomozygous54234736
7120572120120572121TTGGAGGTGACACCCTCAGAGGGGAC25GENIChomozygous54921106
7120572746120572747TTTG23GENIChomozygous54234738
7120572828120572829GT30GENIChomozygous54234740
7120573119120573120GC17GENIChomozygous54234742
7120573214120573215GT16GENIChomozygous54234744
7120573267120573268AC14GENIChomozygous54234746
7120573297120573298GA11GENIChomozygous54234748
7120573529120573530AG5GENIChomozygous54234750
7120573693120573694GT4GENIChomozygous54234752
7120573994120573996TG--11GENICheterozygous55144773
7120574421120574422GC9GENIChomozygous54234754
7120574961120574962CT18GENIChomozygous54234756
7120575287120575288CCT12GENICpossibly homozygous54084620
7120575387120575389TT--12GENIChomozygous54234760
7120575445120575446CT16GENIChomozygous54234762
7120575479120575480TTGC11GENICpossibly homozygous55096110
7120575482120575483AACGCGCGCG18GENIChomozygous55096112
7120576424120576425AATT10GENIChomozygous54084626
7120577440120577441GA21GENIChomozygous54234776
7120577956120577957CT18GENIChomozygous54084627
7120579836120579837AG13GENIChomozygous54234778
7120579928120579929TTA5GENICheterozygous54234780
7120580292120580293AG17GENIChomozygous54084628
7120580646120580647CT19GENIChomozygous54234782
7120581531120581532CT17GENIChomozygous54234784
7120581983120581984C-18GENIChomozygous54234786
7120582244120582245GGAAAAAAAAAAAAAAAA4GENICheterozygous55001740
7120582244120582245GGAAAAA4GENICheterozygous55096114
7120582736120582737GA30GENIChomozygous54234790
7120583783120583784TTG17GENIChomozygous54234792
7120584194120584195GA18GENIChomozygous54234794
7120584589120584590AG17GENIChomozygous54234796
7120584660120584662TT--15GENIChomozygous54084632
7120584810120584811CG24GENIChomozygous54234798
7120584812120584813AT24GENIChomozygous54234800
7120584937120584938AAG21GENIChomozygous54234802
7120585738120585739CT20GENIChomozygous54234804