chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107963003107963004GC20GENIChomozygous141525765
3107964138107964139TA20GENIChomozygous145205791
3107965452107965453TG19GENIChomozygous145205792
3107965520107965521AG26GENIChomozygous141525766
3107966133107966134GA16GENIChomozygous145205793
3107966032107966033AG16GENIChomozygous136784561
3107965120107965121TC22GENIChomozygous136784560
3107966066107966067TC14GENIChomozygous136784562
3107969438107969439CT23GENIChomozygous145205794
3107969564107969565AG22GENIChomozygous145205795
3107969566107969567CT22GENIChomozygous145205796
3107969712107969713AC24GENIChomozygous145205797
3107969873107969874TC19GENIChomozygous145205798
3107969935107969936CT14GENIChomozygous145205799
3107970214107970215AC20GENIChomozygous136784565
3107970781107970782AG19GENIChomozygous136784566
3107971163107971164CT16GENIChomozygous145205800
3107971208107971209GT19GENIChomozygous136784567
3107971382107971383TC20GENIChomozygous136784568
3107971384107971385AT18GENIChomozygous136784569
3107971399107971400CA17GENIChomozygous136784570
3107971401107971402AT18GENIChomozygous136784571
3107971408107971409GT18GENIChomozygous136784572
3107971578107971579TA8GENIChomozygous145205801
3107971762107971763TC14GENIChomozygous145205802
3107972147107972148GA8GENIChomozygous145205803
3107972281107972282TA9GENIChomozygous145205804
3107972362107972363TC15GENIChomozygous145205805
3107972455107972456AT24GENIChomozygous136784575
3107972456107972457TC23GENIChomozygous136784576
3107972627107972628TC17GENIChomozygous145205806
3107972941107972942GC24GENIChomozygous145205807
3107972967107972968GA22GENIChomozygous145205808
3107973315107973316TC10GENIChomozygous145205809
3107973373107973374AC14GENIChomozygous145205810
3107973936107973937TA4GENIChomozygous145205811
3107972749107972749A15GENIChomozygous145204560
3107971782107971782TTTTTTTTTCT6GENIChomozygous145204559
3107972986107972992AAAAAC18GENIChomozygous145204561