chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191064429810644299GA24GENIChomozygous46059619
191064436510644366TC31GENIChomozygous46059620
191064451610644517CT35GENIChomozygous46059621
191064461310644614CT22GENIChomozygous46059622
191064462210644623AG25GENIChomozygous46059623
191064467310644674TC21GENIChomozygous46059624
191064470510644706GA23GENIChomozygous46059625
191064497310644974CT27GENIChomozygous46059626
191064500010645001CT23GENIChomozygous46059627
191064511110645112TC33GENIChomozygous46059628
191064512910645130GA33GENIChomozygous46059629
191064519710645198AG22GENIChomozygous46059630
191064567010645671CT22GENIChomozygous46059631
191064605710646058CT25GENIChomozygous46059632
191064621610646217TC11GENIChomozygous46059633
191064626510646266GA16GENIChomozygous46059634
191064627810646279AC17GENIChomozygous46059635
191064631310646314CCTT10GENICheterozygous46378340
191064637710646378GA40GENIChomozygous46059638
191064673710646738TC33GENIChomozygous46059639
191064674510646746TA34GENIChomozygous46059640
191064719410647202GGGTGGGA--------4GENIChomozygous46059642
191064740510647406TTC28GENIChomozygous46059643
191064767110647672TC27GENICpossibly homozygous46059644
191064768010647681TC26GENICpossibly homozygous46059645
191064820510648206TG22INTERGENIChomozygous46059646
191064832110648322AACC4INTERGENICheterozygous46059647
191064837910648380GC20INTERGENIChomozygous46059648
191065129610651297AC18INTERGENIChomozygous46059650
191065159510651596CT8INTERGENIChomozygous46059651
191065183410651835CT10INTERGENIChomozygous46059653
191065193610651960CTTGCTTGCTTTCTTTCTTTCTTT------------------------7INTERGENIChomozygous46458626
191065223210652233TG21INTERGENIChomozygous46059658
191065257810652579CA27INTERGENIChomozygous46059659
191065306210653063GA24INTERGENIChomozygous46059660
191065325410653255TC31INTERGENIChomozygous46059661
191065337710653378CA28INTERGENIChomozygous46059662