chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176102336176102337TG10GENIChomozygous111841336
3176102701176102702CT25GENIChomozygous112218573
3176102816176102817GA12GENIChomozygous112218574
3176103374176103375AG21GENIChomozygous112218575
3176103386176103387GA24GENIChomozygous112218576
3176103575176103576TC17GENIChomozygous112218577
3176104030176104031TC25GENIChomozygous112218578
3176104070176104071AG30GENIChomozygous112218579
3176104830176104831AG33GENIChomozygous112218580
3176105076176105077TA21GENIChomozygous112218581
3176105119176105120GA15GENIChomozygous112218582
3176105681176105682AG26GENIChomozygous112218583
3176106121176106122GA20GENIChomozygous112218584
3176107498176107499TC24GENIChomozygous112218585
3176107507176107508CA27GENIChomozygous112218586
3176108587176108588TG10GENIChomozygous112218587
3176108922176108923AT17GENIChomozygous112218588
3176111220176111221TC17GENIChomozygous112218589
3176111558176111559GA36GENIChomozygous112218590
3176112118176112119CT17GENIChomozygous112218591
3176115936176115937CT24GENIChomozygous112218592
3176119260176119261TA22GENIChomozygous112218594
3176119574176119575GA23GENIChomozygous112218595
3176119658176119659AG22GENIChomozygous112218596
3176122367176122368AC21GENIChomozygous112218598
3176123555176123556TC17GENIChomozygous112218599
3176124808176124809AC33GENIChomozygous112218600