chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176102336176102337TG47GENIChomozygous111841336
3176102701176102702CT52GENIChomozygous112218573
3176102816176102817GA37GENIChomozygous112218574
3176103374176103375AG43GENIChomozygous112218575
3176103386176103387GA41GENIChomozygous112218576
3176103575176103576TC47GENIChomozygous112218577
3176104030176104031TC49GENIChomozygous112218578
3176104070176104071AG36GENIChomozygous112218579
3176104830176104831AG61GENIChomozygous112218580
3176105076176105077TA62GENIChomozygous112218581
3176105119176105120GA51GENIChomozygous112218582
3176105681176105682AG57GENIChomozygous112218583
3176106121176106122GA45GENIChomozygous112218584
3176107498176107499TC50GENIChomozygous112218585
3176107507176107508CA51GENIChomozygous112218586
3176108587176108588TG62GENIChomozygous112218587
3176108922176108923AT38GENIChomozygous112218588
3176111220176111221TC30GENIChomozygous112218589
3176111558176111559GA44GENIChomozygous112218590
3176112118176112119CT38GENIChomozygous112218591
3176115936176115937CT22GENIChomozygous112218592
3176119260176119261TA44GENIChomozygous112218594
3176119574176119575GA48GENIChomozygous112218595
3176119658176119659AG37GENIChomozygous112218596
3176122367176122368AC18GENIChomozygous112218598
3176123555176123556TC25GENIChomozygous112218599
3176124808176124809AC19GENIChomozygous112218600