chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1133740885133740886TC33GENIChomozygous62298767
1133741328133741329TC31GENIChomozygous62298768
1133741383133741384TC28GENIChomozygous62298769
1133741407133741408TC31GENIChomozygous62298770
1133741538133741554ATATATATATATATAT----------------25GENICheterozygous62549047
1133741611133741612AG35GENIChomozygous62298771
1133741731133741732TC30GENIChomozygous62298772
1133742565133742566AG41GENIChomozygous62298773
1133742611133742612GC39GENIChomozygous62298774
1133742752133742753AAC32GENIChomozygous62298775
1133743002133743003AG45GENIChomozygous62298776
1133743016133743017T-44GENIChomozygous62298777
1133743613133743614GA33GENIChomozygous62298778
1133744201133744202TC34GENIChomozygous62298779
1133744237133744238GA38GENICpossibly homozygous62298780
1133744608133744609AT26GENIChomozygous62298781
1133744719133744720AG28GENIChomozygous62298782
1133745031133745032TC31GENIChomozygous62298783
1133745316133745317T-24GENIChomozygous62298784
1133745397133745398TC28GENIChomozygous62298785
1133741540133741554ATATATATATATAT--------------25GENICpossibly homozygous62543635
1133747576133747577TTA37GENIChomozygous60854188
1133747943133747944GC11GENIChomozygous60854193
1133748106133748107C-36GENIChomozygous60854196
1133748319133748320CT32GENIChomozygous62298790
1133751590133751591GA28GENIChomozygous62298792
1133747954133747958AGCA----9GENIChomozygous62246398