chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----20GENIChomozygous693800821
3154514276154514277TG23GENIChomozygous528995123
3154514414154514415AAGTCT9GENIChomozygous693800822
3154514475154514476TC19GENIChomozygous528995124
3154514477154514478TC19GENIChomozygous528995125
3154515475154515476GA12GENIChomozygous528995126
3154515681154515682TA27GENIChomozygous528995127
3154516260154516261TC23GENIChomozygous528995128
3154516884154516885AG33GENIChomozygous528995129
3154517077154517078TC21GENIChomozygous531278937
3154517156154517157AG16GENIChomozygous528995130
3154517593154517594TC23GENIChomozygous528995131
3154517632154517633G-19GENIChomozygous693800823
3154517898154517899TC18GENIChomozygous528995132
3154517982154517986GGCA----17GENIChomozygous693800824
3154518068154518069GA20GENIChomozygous528995133
3154518158154518159TTA16GENIChomozygous693800825
3154518562154518563CT13GENIChomozygous531278938
3154518737154518738AG13GENIChomozygous528995134
3154518931154518932GGT11GENICpossibly homozygous693800826
3154519100154519101CT14GENIChomozygous531278939
3154519184154519185CCA12GENIChomozygous693800827
3154519315154519316CT21GENIChomozygous528995135
3154519630154519636TCCCTC------15GENICheterozygous693800829
3154519645154519646CG30GENICpossibly homozygous528995136
3154519651154519652GC30GENICpossibly homozygous528995137
3154519896154519897CCTT11GENICheterozygous693800831
3154519897154519899TT--11GENICheterozygous693800830
3154519985154519986AG21GENIChomozygous528995138
3154520058154520059TC24GENIChomozygous528995139
3154520781154520782TC27GENIChomozygous528995140
3154520987154520988CT32GENIChomozygous528995141
3154521914154521915TTAA5GENIChomozygous693800832
3154521930154521931AAC5GENICheterozygous693800833
3154522134154522135AG7GENIChomozygous528995142