chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166934174166934175G25GENIChomozygous128269353
5166934223166934224G31GENIChomozygous128269354
5166934239166934239T36GENIChomozygous128269355
5166934262166934262T44GENIChomozygous128269356
5166934267166934267A46GENIChomozygous128269357
5166934321166934321C45GENIChomozygous128269358
5166934356166934356T45GENIChomozygous128269359
5166934422166934424CA21GENICheterozygous128269360
5166934463166934464A26GENIChomozygous128269361
5166934504166934505G26GENIChomozygous128269362
5166934534166934534T27GENIChomozygous128269363
5166934559166934560A30GENIChomozygous128269364
5166934575166934575C35GENIChomozygous128269365
5166934666166934667T35GENIChomozygous128269366
5166934759166934760C44GENIChomozygous128269367
5166936926166936926A14GENIChomozygous128269368
5166956847166956847C40GENIChomozygous128269369
5166956885166956885G36GENIChomozygous128269372
5166956866166956866C40GENIChomozygous128269370
5166956880166956881G38GENIChomozygous128269371
5166956924166956924GT40GENIChomozygous128269373
5166956969166956970C43GENIChomozygous128269374
5166966877166966879AG29GENICheterozygous128269375
5166969721166969722G23GENICheterozygous128269376
5166956946166956947GT41GENIChomozygous118847666
5166956947166956948TG42GENIChomozygous114162826
5166956963166956964AC45GENIChomozygous114082168