chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116037212660372127AG26GENICheterozygous50795395
116037218060372181CT32GENICheterozygous50795396
116037228960372290GA43GENICheterozygous50795398
116038119160381192AG11GENICheterozygous50795430
116039248360392484TC6GENICheterozygous50795479
116039854560398546TC8GENICheterozygous50795507
116039876260398763AG34GENICheterozygous50795509
116039884460398845CT35GENICheterozygous50795510
116039889060398891CA20GENICheterozygous50795512
116041103560411036GA24GENICheterozygous50795660
116041109360411094GA20GENICheterozygous50795662
116041774760417748GC16GENICheterozygous50795736
116041785860417859TC27GENICheterozygous50795738
116041804560418046AC38GENICheterozygous50795740
116041840560418406AG28GENICheterozygous50795742
116041883860418839AG29GENICheterozygous50795744
116041898560418986GA49GENICheterozygous50795746
116041902460419025TC50GENICheterozygous50795747
116041931160419312GA19GENICheterozygous50795749
116041952060419521AG18GENICheterozygous50795751
116041954860419549GA23GENICheterozygous50795753
116041958560419587GG--24GENICheterozygous50795755
116041959460419595GA25GENICheterozygous50795757
116041979960419800C-49GENICheterozygous50795759
116041986260419863CT45GENICheterozygous50795761
116042013560420136GC20GENICheterozygous50795763
116042014760420148TA22GENICheterozygous50795765
116042051960420520TC50GENICheterozygous50795766
116042052860420529GA50GENICheterozygous50795768
116042108760421088CCA29GENICheterozygous50795770
116042162560421626CT38GENICheterozygous50795776
116042196760421968GA49GENICheterozygous50795778
116042273460422735TC40GENICheterozygous50795787
116042284560422846AG33GENICheterozygous50795789
116042286360422864GT37GENICheterozygous50795791
116042309260423093AT33GENICheterozygous50795793
116042309960423100CT33GENICheterozygous50795795
116042346160423462CCT24GENICheterozygous50795798