chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3176102336176102337TG49GENIChomozygous111841336
3176103575176103576TC47GENIChomozygous112218577
3176102816176102817GA53GENIChomozygous112218574
3176102701176102702CT66GENIChomozygous112218573
3176103374176103375AG61GENIChomozygous112218575
3176103386176103387GA57GENIChomozygous112218576
3176104030176104031TC45GENIChomozygous112218578
3176104070176104071AG43GENIChomozygous112218579
3176104830176104831AG48GENIChomozygous112218580
3176105076176105077TA60GENIChomozygous112218581
3176105119176105120GA54GENIChomozygous112218582
3176105681176105682AG64GENIChomozygous112218583
3176106121176106122GA51GENIChomozygous112218584
3176107498176107499TC52GENICpossibly homozygous112218585
3176107507176107508CA51GENIChomozygous112218586
3176108587176108588TG36GENIChomozygous112218587
3176108922176108923AT40GENIChomozygous112218588
3176111220176111221TC37GENIChomozygous112218589
3176111558176111559GA68GENIChomozygous112218590
3176112118176112119CT46GENIChomozygous112218591
3176115936176115937CT44GENIChomozygous112218592
3176119260176119261TA65GENIChomozygous112218594
3176119574176119575GA49GENIChomozygous112218595
3176119658176119659AG40GENIChomozygous112218596
3176122367176122368AC56GENIChomozygous112218598
3176109877176109877T68GENIChomozygous130916825
3176119798176119798AAAC38GENIChomozygous130916826
3176122114176122114G43GENIChomozygous130916827
3176122923176122924A53GENIChomozygous127965216
3176122920176122920G53GENIChomozygous127965215
3176103729176103729CACTCA45GENIChomozygous127965213
3176123114176123114ATGTACACGTACCACAGAACTAACGTAGGGATTAGAGGGCAACTTTGTGGAGTCAGTTCTCTTCTAATTTTACGTGGGTCCTGGACATTAAATTCGAGTTACCAGACTGGAGCAA7GENIChomozygous127965217
3176123159176123166TTGATGT51GENIChomozygous130916828
3176123555176123556TC52GENIChomozygous112218599
3176124808176124809AC50GENIChomozygous112218600