chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----13GENIChomozygous688892769
3154514276154514277TG17GENIChomozygous515910625
3154514414154514415AAGTCT23GENIChomozygous688892770
3154514475154514476TC22GENIChomozygous515910626
3154514477154514478TC22GENIChomozygous515910627
3154515475154515476GA18GENIChomozygous515910628
3154515681154515682TA28GENIChomozygous515910629
3154516008154516009GA29GENIChomozygous515910630
3154516009154516010AT29GENIChomozygous515910631
3154516260154516261TC27GENIChomozygous515910632
3154516884154516885AG28GENIChomozygous515910633
3154517077154517078TC36GENIChomozygous518213129
3154517156154517157AG22GENIChomozygous515910634
3154517593154517594TC16GENIChomozygous515910635
3154517632154517633G-21GENIChomozygous688892771
3154517898154517899TC27GENIChomozygous515910636
3154517982154517986GGCA----26GENIChomozygous688892772
3154518068154518069GA40GENIChomozygous515910637
3154518158154518159TTA34GENIChomozygous688892773
3154518562154518563CT30GENIChomozygous518213130
3154518737154518738AG33GENIChomozygous515910638
3154518931154518932GGT17GENICpossibly homozygous688892774
3154519100154519101CT23GENIChomozygous518213131
3154519184154519185CCA19GENIChomozygous688892775
3154519315154519316CT36GENIChomozygous515910639
3154519630154519636TCCCTC------15GENICheterozygous688892777
3154519645154519646CG24GENIChomozygous515910640
3154519651154519652GC24GENIChomozygous515910641
3154519896154519897CCTT18GENICpossibly homozygous688892779
3154519985154519986AG32GENIChomozygous515910642
3154520058154520059TC32GENIChomozygous515910643
3154520781154520782TC28GENIChomozygous515910644
3154520987154520988CT27GENIChomozygous515910645
3154521914154521915TTAA9GENICpossibly homozygous688892780
3154521930154521931AAC11GENICheterozygous688892781
3154521931154521932AC10GENICheterozygous515910646
3154522134154522135AG22GENIChomozygous515910647