chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166917688166917690AC38GENICheterozygous130316546
5166934267166934267A37GENIChomozygous128269357
5166934174166934175G21GENIChomozygous128269353
5166934223166934224G22GENIChomozygous128269354
5166934239166934239T30GENIChomozygous128269355
5166934262166934262T35GENIChomozygous128269356
5166934463166934464A19GENIChomozygous128269361
5166934504166934505G24GENIChomozygous128269362
5166934534166934534T32GENIChomozygous128269363
5166934559166934560A31GENIChomozygous128269364
5166934575166934575C30GENIChomozygous128269365
5166934666166934667T47GENIChomozygous128269366
5166934759166934760C49GENIChomozygous128269367
5166936926166936926A26GENICpossibly homozygous128269368
5166946856166946858AC36GENICheterozygous130316547
5166956847166956847C24GENIChomozygous128269369
5166956866166956866C32GENIChomozygous128269370
5166956880166956881G31GENIChomozygous128269371
5166956885166956885G31GENIChomozygous128269372
5166956924166956924GT37GENIChomozygous128269373
5166956947166956948TG40GENIChomozygous114162826
5166956963166956964AC42GENIChomozygous114082168
5166956969166956970C44GENIChomozygous128269374
5166966843166966845AG28GENICheterozygous130316548
5166966877166966879AG34GENICheterozygous128269375
5166969721166969722G22GENICheterozygous128269376
5166974370166974370A37GENICheterozygous130316549
5166934356166934356T31GENIChomozygous128269359
5166956946166956947GT40GENIChomozygous118847666
5166934321166934321C34GENIChomozygous128269358