chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107963003107963004GC24GENIChomozygous141525765
3107964138107964139TA16GENIChomozygous145205791
3107965452107965453TG24GENIChomozygous145205792
3107965520107965521AG19GENIChomozygous141525766
3107966133107966134GA18GENIChomozygous145205793
3107965120107965121TC15GENIChomozygous136784560
3107966032107966033AG11GENIChomozygous136784561
3107966066107966067TC13GENIChomozygous136784562
3107969438107969439CT18GENIChomozygous145205794
3107969564107969565AG15GENIChomozygous145205795
3107969566107969567CT16GENIChomozygous145205796
3107969712107969713AC24GENIChomozygous145205797
3107969873107969874TC22GENIChomozygous145205798
3107969935107969936CT19GENIChomozygous145205799
3107970214107970215AC16GENIChomozygous136784565
3107970781107970782AG12GENIChomozygous136784566
3107971163107971164CT16GENIChomozygous145205800
3107971208107971209GT18GENIChomozygous136784567
3107971382107971383TC13GENIChomozygous136784568
3107971384107971385AT13GENIChomozygous136784569
3107971399107971400CA14GENIChomozygous136784570
3107971401107971402AT15GENIChomozygous136784571
3107971408107971409GT15GENIChomozygous136784572
3107971578107971579TA17GENICpossibly homozygous145205801
3107971762107971763TC18GENIChomozygous145205802
3107972147107972148GA18GENIChomozygous145205803
3107972281107972282TA17GENIChomozygous145205804
3107972362107972363TC20GENIChomozygous145205805
3107972455107972456AT14GENIChomozygous136784575
3107972456107972457TC14GENIChomozygous136784576
3107972627107972628TC22GENIChomozygous145205806
3107972941107972942GC10GENIChomozygous145205807
3107972967107972968GA10GENIChomozygous145205808
3107972986107972992AAAAAC10GENIChomozygous145204561
3107971782107971782TTTTTTTTTCT7GENICpossibly homozygous145204559
3107972749107972749A20GENIChomozygous145204560
3107973315107973316TC18GENIChomozygous145205809
3107973373107973374AC20GENIChomozygous145205810
3107973936107973937TA12GENIChomozygous145205811