chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7138947494138947495TC32GENICheterozygous522475962
7138947534138947535GA51GENIChomozygous521715309
7138947566138947567GGT48GENICheterozygous690917752
7138947570138947571A-44GENICheterozygous690917753
7138947582138947583TC52GENIChomozygous521715310
7138947619138947620GT50GENIChomozygous521715311
7138947697138947698CT72GENICheterozygous522475963
7138947754138947755GA59GENICheterozygous522475964
7138947817138947818GC19GENICheterozygous522475965
7138947845138947846TC11GENIChomozygous522475966
7138947865138947866GA12GENICheterozygous522475967
7138947880138947881GA13GENICheterozygous522475968
7138948029138948030GA8GENIChomozygous522475969
7138948199138948200AG19GENIChomozygous521715312
7138948227138948228AAG6GENIChomozygous690917754
7138948229138948230TTTGAG4GENIChomozygous690917755
7138948233138948234GGT1GENIChomozygous690917756
7138948245138948246T-1GENIChomozygous690917757
7138948350138948351CT15GENICpossibly homozygous521715313
7138948620138948621CA24GENICpossibly homozygous521715314
7138948642138948643AG23GENIChomozygous521715315
7138948653138948654AG28GENIChomozygous521715316
7138948877138948878TA29GENICpossibly homozygous521715317
7138948908138948909GC26GENIChomozygous521715318
7138948930138948931TC31GENIChomozygous521715319
7138948935138948936CG31GENIChomozygous521715320
7138949108138949109CA35GENIChomozygous521715321
7138949121138949122TC30GENIChomozygous521715322
7138949149138949150CT23GENIChomozygous521715323
7138949181138949182AG35GENIChomozygous521715324
7138949385138949386GC35GENIChomozygous521715325
7138949491138949492GT25GENIChomozygous521715326
7138949614138949615AG11GENIChomozygous522475970
7138949631138949632GA10GENIChomozygous521715327
7138949633138949634TC11GENIChomozygous521715328
7138949680138949681TC9GENIChomozygous521715329
7138949737138949738AG9GENICheterozygous521715330