chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2050713905071391GT36GENIChomozygous109076435
2050714945071495TA21GENIChomozygous109076437
2050716595071660CT23GENIChomozygous109076439
2050719465071947TC27GENIChomozygous109076441
2050721845072185GT32GENIChomozygous109233788
2050722105072211GA28GENICpossibly homozygous109329659
2050722555072256AG35GENIChomozygous109329661
2050724255072426TC45GENICpossibly homozygous119763410
2050724435072444GC38GENICpossibly homozygous119763411
2050724485072449CT37GENICpossibly homozygous119763412
2050724665072467TC33GENIChomozygous119763413
2050725085072509CT16GENIChomozygous119763414
2050725565072557TC22GENIChomozygous109605719
2050725715072572CG25GENIChomozygous109233789
2050728915072892AT20GENIChomozygous109076443
2050729945072995GA19GENIChomozygous109076445
2050729985072999AT19GENIChomozygous109076447
2050730035073004CT20GENIChomozygous109076449
2050730105073011CT18GENIChomozygous109076451
2050730125073013AC18GENIChomozygous109076453
2050734025073403GA16GENICheterozygous109233790
2050734425073443TC15GENIChomozygous109076455
2050735145073515TC29GENIChomozygous109076457
2050738665073867GA22GENIChomozygous109076459
2050743675074368GT23GENIChomozygous109076461
2050745125074513GA31GENIChomozygous109076467
2050746065074607AG29GENIChomozygous109076469
2050750585075059GT28GENIChomozygous109076471
2050750655075066GA26GENIChomozygous109076473
2050754515075452GA25GENIChomozygous109233792
2050756105075611AG23GENIChomozygous109233793
2050756835075684AG27GENIChomozygous109076475
2050756985075699CT28GENIChomozygous109233794
2050758985075899GA22GENIChomozygous109076477
2050759085075909GA22GENIChomozygous109076479
2050762525076253CT21GENICpossibly homozygous109542195
2050762825076283AG17GENIChomozygous109076481
2050763545076355AG21GENIChomozygous109076483
2050763895076390TC24GENIChomozygous109076485
2050765095076510AG34GENICpossibly homozygous109076489
2050765435076544GA24GENICpossibly homozygous109329663