chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3154514251154514255CGGC----22GENIChomozygous695433324
3154514276154514277TG36GENIChomozygous533340467
3154514414154514415AAGTCT33GENIChomozygous695433325
3154514475154514476TC25GENIChomozygous533340468
3154514477154514478TC25GENIChomozygous533340469
3154515475154515476GA33GENIChomozygous533340470
3154515681154515682TA51GENIChomozygous533340471
3154516008154516009GA54GENICpossibly homozygous533340472
3154516009154516010AT53GENIChomozygous533340473
3154516260154516261TC31GENIChomozygous533340474
3154516884154516885AG54GENIChomozygous533340475
3154517077154517078TC64GENIChomozygous535822443
3154517156154517157AG52GENICpossibly homozygous533340476
3154517593154517594TC40GENIChomozygous533340477
3154517632154517633G-32GENIChomozygous695433326
3154517898154517899TC44GENIChomozygous533340478
3154517982154517986GGCA----25GENIChomozygous695433327
3154518068154518069GA40GENIChomozygous533340479
3154518158154518159TTA53GENIChomozygous695433328
3154518562154518563CT54GENIChomozygous535822444
3154518737154518738AG52GENIChomozygous533340480
3154518931154518932GGT25GENIChomozygous695433329
3154519100154519101CT35GENICpossibly homozygous535822445
3154519184154519185CCA19GENIChomozygous695433330
3154519315154519316CT45GENICpossibly homozygous533340481
3154519630154519636TCCCTC------18GENICheterozygous695433332
3154519645154519646CG32GENIChomozygous533340482
3154519651154519652GC36GENIChomozygous533340483
3154519896154519897CCTT14GENIChomozygous695433334
3154519985154519986AG51GENICpossibly homozygous533340484
3154520058154520059TC49GENIChomozygous533340485
3154520781154520782TC35GENIChomozygous533340486
3154520987154520988CT28GENIChomozygous533340487
3154521914154521915TTAA16GENIChomozygous695433335
3154521930154521931AAC19GENICheterozygous695433336
3154521931154521932AC23GENICheterozygous533340488
3154522134154522135AG37GENIChomozygous533340489