chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----1GENIChomozygous717518419
3154514276154514277TG9GENIChomozygous578668125
3154514414154514415AAGTCT9GENIChomozygous717518421
3154514475154514476TC10GENIChomozygous578668126
3154514477154514478TC10GENIChomozygous578668127
3154515475154515476GA12GENIChomozygous578668128
3154515681154515682TA18GENICheterozygous578668129
3154516008154516009GA6GENIChomozygous578668130
3154516009154516010AT6GENIChomozygous578668131
3154516260154516261TC16GENICheterozygous578668132
3154516884154516885AG15GENICpossibly homozygous578668133
3154517077154517078TC21GENICpossibly homozygous580613403
3154517156154517157AG28GENIChomozygous578668134
3154517593154517594TC11GENICpossibly homozygous578668135
3154517632154517633G-9GENIChomozygous717518423
3154517898154517899TC22GENIChomozygous578668136
3154517982154517986GGCA----8GENIChomozygous717518424
3154518068154518069GA14GENIChomozygous578668137
3154518158154518159TTA19GENICpossibly homozygous717518425
3154518562154518563CT25GENIChomozygous580613404
3154518737154518738AG22GENICpossibly homozygous578668138
3154519100154519101CT24GENIChomozygous580613405
3154519184154519185CCA8GENICheterozygous717518426
3154519184154519185CCCA8GENICheterozygous717518427
3154519315154519316CT32GENICpossibly homozygous578668139
3154519985154519986AG12GENICpossibly homozygous578668140
3154520058154520059TC20GENIChomozygous578668141
3154520781154520782TC16GENICpossibly homozygous578668142
3154520987154520988CT15GENICpossibly homozygous578668143
3154522134154522135AG22GENICpossibly homozygous578668144