chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----28GENIChomozygous683761755
3154514276154514277TG33GENIChomozygous502156237
3154514414154514415AAGTCT30GENIChomozygous683761756
3154514475154514476TC36GENIChomozygous502156238
3154514477154514478TC37GENIChomozygous502156239
3154515475154515476GA50GENIChomozygous502156240
3154515681154515682TA50GENIChomozygous502156241
3154516008154516009GA43GENIChomozygous502156242
3154516009154516010AT43GENIChomozygous502156243
3154516260154516261TC56GENIChomozygous502156244
3154516884154516885AG41GENIChomozygous502156245
3154517077154517078TC42GENIChomozygous504667214
3154517156154517157AG24GENIChomozygous502156246
3154517593154517594TC35GENIChomozygous502156247
3154517632154517633G-25GENIChomozygous683761757
3154517898154517899TC48GENIChomozygous502156248
3154517982154517986GGCA----50GENIChomozygous683761758
3154518068154518069GA52GENIChomozygous502156249
3154518158154518159TTA57GENIChomozygous683761759
3154518562154518563CT78GENIChomozygous504667215
3154518737154518738AG68GENIChomozygous502156250
3154518931154518932GGT26GENIChomozygous683761760
3154519100154519101CT43GENIChomozygous504667216
3154519184154519185CCA15GENIChomozygous683761761
3154519315154519316CT41GENICpossibly homozygous502156251
3154519630154519636TCCCTC------41GENICheterozygous683761763
3154519645154519646CG52GENICpossibly homozygous502156252
3154519651154519652GC46GENICpossibly homozygous502156253
3154519896154519897CCTT16GENIChomozygous683761765
3154519985154519986AG38GENIChomozygous502156254
3154520058154520059TC31GENIChomozygous502156255
3154520781154520782TC34GENIChomozygous502156256
3154520987154520988CT56GENIChomozygous502156257
3154521914154521915TTAA15GENIChomozygous683761766
3154521930154521931AAC25GENICheterozygous683761767
3154522134154522135AG61GENIChomozygous502156258