chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178054734380547344AAT17GENIChomozygous753106050
178054735380547354GGT15GENIChomozygous753106051
178054740980547410A-7GENICpossibly homozygous753106053
178054782680547827GT19GENICpossibly homozygous643343277
178054822380548224TC26GENIChomozygous643343278
178054851780548518CT24GENIChomozygous643343279
178054916980549170AG21GENIChomozygous643343280
178054917280549173GA23GENIChomozygous643343281
178054927280549273TC10GENIChomozygous643343282
178054940680549407GA16GENIChomozygous643343283
178055011880550120TT--5GENIChomozygous753106057
178055013880550139GT14GENIChomozygous643343284
178055212080552121GC21GENIChomozygous643343285
178055212980552130GT20GENIChomozygous643343286
178055216980552170CCCT14GENIChomozygous753106059
178055227680552277AG26GENIChomozygous643343287
178055231180552312CA21GENIChomozygous643343288
178055245780552458CT34GENIChomozygous643343289
178055270180552702GGCTCGTCA34GENICpossibly homozygous753106060
178055285980552860C-19GENIChomozygous753106061
178055286680552867CT20GENIChomozygous643343290
178055357080553571CCAA9GENICpossibly homozygous753106063
178055357080553571CCAAAA9GENICheterozygous753106064
178055390680553907AG26GENIChomozygous643343291
178055408680554087CCT8GENIChomozygous753106065
178055409480554095CG11GENIChomozygous643343292
178055410380554104CA13GENIChomozygous643343293
178055428880554289AG21GENIChomozygous643343294
178055434780554348TTA18GENIChomozygous753106066
178055442480554425GGA21GENICpossibly homozygous753106067
178055444480554445AC25GENIChomozygous643343295