chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----9GENIChomozygous697081486
3154514276154514277TG13GENIChomozygous537789842
3154514414154514415AAGTCT14GENIChomozygous697081487
3154514475154514476TC16GENIChomozygous537789843
3154514477154514478TC15GENIChomozygous537789844
3154515475154515476GA15GENIChomozygous537789845
3154515681154515682TA45GENIChomozygous537789846
3154516009154516010AT32GENIChomozygous537789847
3154516260154516261TC26GENIChomozygous537789848
3154516884154516885AG38GENIChomozygous537789849
3154517077154517078TC28GENIChomozygous540178527
3154517156154517157AG18GENIChomozygous537789850
3154517593154517594TC28GENIChomozygous537789851
3154517632154517633G-24GENIChomozygous697081488
3154517898154517899TC26GENIChomozygous537789852
3154517982154517986GGCA----24GENIChomozygous697081489
3154518068154518069GA37GENIChomozygous537789853
3154518158154518159TTA58GENIChomozygous697081490
3154518562154518563CT41GENIChomozygous540178528
3154518737154518738AG24GENIChomozygous537789854
3154518931154518932GGT14GENICpossibly homozygous697081491
3154519100154519101CT20GENIChomozygous540178529
3154519184154519185CCA21GENIChomozygous697081492
3154519315154519316CT26GENIChomozygous537789855
3154519630154519636TCCCTC------20GENICheterozygous697081494
3154519645154519646CG37GENIChomozygous537789856
3154519651154519652GC37GENIChomozygous537789857
3154519896154519897CCTT11GENIChomozygous697081496
3154519985154519986AG37GENIChomozygous537789858
3154520058154520059TC27GENICpossibly homozygous537789859
3154520781154520782TC35GENIChomozygous537789860
3154520987154520988CT28GENIChomozygous537789861
3154521914154521915TTAA4GENIChomozygous697081497
3154521930154521931AAC6GENICheterozygous697081498
3154522134154522135AG39GENIChomozygous537789862