chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7125746090125746091CT28GENIChomozygous649064813
7125747342125747343CT15GENIChomozygous649064814
7125747534125747535CT11GENIChomozygous649064815
7125747571125747572GA15GENIChomozygous649064816
7125748329125748330AG27GENIChomozygous649064817
7125748832125748833C-4GENIChomozygous756522239
7125748927125748928GA27GENIChomozygous649064818
7125749012125749013GA26GENIChomozygous649064819
7125749414125749415AG24GENIChomozygous649064820
7125751521125751522AAT18GENICheterozygous756522240
7125751521125751522AATT18GENICheterozygous756522241
7125752000125752001TC22GENIChomozygous649064821
7125752756125752757GA17GENIChomozygous649064822
7125753821125753822CT13GENIChomozygous649064823
7125753897125753898CT21GENIChomozygous649064824
7125753949125753950GA41GENIChomozygous649064825
7125754274125754275AG29GENIChomozygous649064826
7125754320125754321CT27GENIChomozygous649064827
7125754367125754368CT23GENIChomozygous649064828
7125754379125754380GC27GENIChomozygous649064829
7125755157125755158GA3GENIChomozygous649064830
7125755666125755667CT24GENIChomozygous649064831
7125755703125755704CT23GENIChomozygous649064832
7125756500125756501TC14GENIChomozygous649064833
7125756849125756850AG12GENIChomozygous649064834
7125756965125756966GGAAAA8GENICheterozygous756522243
7125756965125756966GGAAAAAAAAAAA8GENICheterozygous756522244
7125757153125757154TTA17GENIChomozygous756522245