chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96995862169958622TC4GENIChomozygous120416903
96995890669958907CT3GENIChomozygous120401218
96995915169959152TG10GENIChomozygous120401219
96995919669959197CT9GENIChomozygous120416904
96995926869959269GA5GENIChomozygous120416905
96995954469959545GA6GENIChomozygous120416906
96996253369962534GC3GENIChomozygous120401226
96996371269963713AG2GENIChomozygous120401228
96996412469964125CA7GENIChomozygous120455373
96996563169965632TC4GENIChomozygous120455374
96996731769967318TC8GENIChomozygous120401229
96996883769968838GA5GENIChomozygous120455375
96996937169969372AG5GENIChomozygous120416911
96996944469969445GA12GENIChomozygous120455376
96996967969969680AT7GENIChomozygous120416912
96997124769971248AG2GENIChomozygous120416913
96997269669972697AG3GENIChomozygous120401230
96997383569973836TA7GENIChomozygous120401232
96997398169973982AG12GENIChomozygous120455377
96997491069974911GA2GENIChomozygous120455378
96997670069976701TC2GENIChomozygous120401235
96997719769977198CT6GENIChomozygous120416916
96998396069983961CT6GENIChomozygous120463041
96998923569989236CG4GENIChomozygous120401240