chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1166031252166031272GCCTTGCGCTCGCTAGGCAA45GENIChomozygous127453278
1166031659166031660AG55GENIChomozygous108355980
1166032837166032838TG60GENIChomozygous108355981
1166033099166033099CAT43GENICpossibly homozygous127453279
1166033538166033539CT58GENIChomozygous108355982
1166033544166033545C58GENIChomozygous127453280
1166033956166033957TC74GENIChomozygous108355983
1166034463166034464AG56GENIChomozygous108355984
1166034474166034475GA58GENIChomozygous108355985
1166034506166034507C59GENIChomozygous127453281
1166034841166034842GA56GENIChomozygous108355986
1166035030166035031A33GENIChomozygous127453282
1166035059166035059T25GENIChomozygous127453283
1166036771166036772TC60GENIChomozygous108355987
1166037823166037824GT50GENIChomozygous109342209
1166033620166033621AG49GENIChomozygous109342201
1166034800166034801GA61GENIChomozygous109342203
1166035096166035097CT20GENIChomozygous109342205
1166035830166035831CT54GENIChomozygous109342207
1166038099166038100TC56GENIChomozygous108355988
1166038102166038103AG57GENIChomozygous108355989
1166038566166038567CT29GENIChomozygous108355990
1166038751166038752CT56GENIChomozygous109342211
1166038756166038757AG56GENIChomozygous109342213
1166039394166039395TC53GENIChomozygous108355991
1166040885166040886AG55GENIChomozygous108355992
1166041051166041051GTGTGTGTGA47GENIChomozygous127453284
1166041095166041096AG42GENIChomozygous108355994
1166041868166041869CT62GENIChomozygous108355996
1166043101166043101CTCT49GENIChomozygous127453285
1166043441166043442GA72GENIChomozygous108355997
1166043557166043557CACCCAAA52GENIChomozygous127453286
1166043558166043558GCA54GENIChomozygous127453287
1166043950166043951AG67GENIChomozygous108355998
1166044017166044018CT68GENIChomozygous109342215
1166044740166044740TT40GENIChomozygous127453288
1166044913166044914CT43GENIChomozygous109342217
1166044972166044973GA44GENIChomozygous108355999