chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3107963003107963004GC15GENIChomozygous141525765
3107964138107964139TA22GENIChomozygous145205791
3107965452107965453TG14GENIChomozygous145205792
3107965520107965521AG16GENIChomozygous141525766
3107966133107966134GA15GENIChomozygous145205793
3107965120107965121TC13GENIChomozygous136784560
3107966032107966033AG12GENIChomozygous136784561
3107966066107966067TC10GENIChomozygous136784562
3107969438107969439CT14GENIChomozygous145205794
3107969564107969565AG15GENIChomozygous145205795
3107969566107969567CT15GENIChomozygous145205796
3107969712107969713AC18GENIChomozygous145205797
3107969873107969874TC17GENIChomozygous145205798
3107969935107969936CT21GENIChomozygous145205799
3107970214107970215AC18GENIChomozygous136784565
3107970781107970782AG20GENIChomozygous136784566
3107971163107971164CT26GENIChomozygous145205800
3107971208107971209GT22GENIChomozygous136784567
3107971382107971383TC14GENIChomozygous136784568
3107971384107971385AT14GENIChomozygous136784569
3107971399107971400CA14GENIChomozygous136784570
3107971401107971402AT14GENIChomozygous136784571
3107971408107971409GT12GENIChomozygous136784572
3107971578107971579TA13GENIChomozygous145205801
3107971762107971763TC10GENIChomozygous145205802
3107972147107972148GA6GENIChomozygous145205803
3107972281107972282TA16GENIChomozygous145205804
3107972362107972363TC22GENIChomozygous145205805
3107972455107972456AT13GENIChomozygous136784575
3107972456107972457TC13GENIChomozygous136784576
3107972627107972628TC15GENIChomozygous145205806
3107972749107972749A15GENIChomozygous145204560
3107971782107971782TTTTTTTTTCT7GENIChomozygous145204559
3107972941107972942GC23GENIChomozygous145205807
3107972967107972968GA18GENIChomozygous145205808
3107972986107972992AAAAAC13GENIChomozygous145204561
3107973315107973316TC18GENIChomozygous145205809
3107973373107973374AC22GENIChomozygous145205810
3107973936107973937TA11GENIChomozygous145205811