chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166934174166934175G11GENIChomozygous128269353
5166934223166934224G9GENIChomozygous128269354
5166934239166934239T13GENIChomozygous128269355
5166934262166934262T22GENIChomozygous128269356
5166934267166934267A21GENIChomozygous128269357
5166934321166934321C21GENIChomozygous128269358
5166934356166934356T21GENIChomozygous128269359
5166934504166934505G10GENIChomozygous128269362
5166934534166934534T10GENIChomozygous128269363
5166934559166934560A13GENIChomozygous128269364
5166934575166934575C15GENIChomozygous128269365
5166934666166934667T18GENIChomozygous128269366
5166934759166934760C20GENIChomozygous128269367
5166936926166936926A8GENICheterozygous128269368
5166936927166936928CA8GENICheterozygous129924406
5166956847166956847C13GENIChomozygous128269369
5166956866166956866C14GENIChomozygous128269370
5166956880166956881G12GENIChomozygous128269371
5166956885166956885G13GENIChomozygous128269372
5166956924166956924GT13GENIChomozygous128269373
5166956947166956948TG13GENIChomozygous114162826
5166956963166956964AC14GENIChomozygous114082168
5166956969166956970C15GENIChomozygous128269374
5166956946166956947GT13GENIChomozygous118847666