chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
183141772331417724TA29GENIChomozygous110322647
183141929131419292AT24GENIChomozygous110322649
183141995331419954GT32GENIChomozygous110322651
183142004331420044AT35GENIChomozygous110322653
183142022331420224AG30GENIChomozygous110322655
183142042531420426GC28GENIChomozygous110322657
183142047231420473GA32GENIChomozygous110322659
183142053531420536AC37GENIChomozygous110322661
183142064131420642CG33GENIChomozygous110322663
183142074531420746CT28GENIChomozygous110744971
183142135831421359TC25GENIChomozygous110322665
183142135931421360TC25GENIChomozygous110322667
183142137531421376GA25GENIChomozygous110322669
183142137631421377GA25GENIChomozygous110322671
183142214431422145GA18GENIChomozygous110322674
183142226531422266AT30GENIChomozygous110322676
183142127231421273TC10GENIChomozygous119487828
183142288331422884CG42GENIChomozygous110322682
183142288731422888CG41GENIChomozygous110322684
183142329031423291TC22GENIChomozygous110322686
183142331731423318AG29GENIChomozygous110322688
183142333831423339CT32GENIChomozygous110322690
183142372431423725TG31GENIChomozygous110322692
183142408331424084TC22GENIChomozygous110322694
183142409731424098AG22GENIChomozygous110322696
183142454131424542CT43GENIChomozygous110322698
183142538931425390TC22GENIChomozygous110322701
183142571931425720TC23GENIChomozygous110322703
183142626131426262AG40GENIChomozygous110322705
183142750031427501GA17GENIChomozygous110322707
183142752931427530CT24GENIChomozygous110322709
183142871131428712CT38GENIChomozygous110322711
183142884731428848AG44GENIChomozygous110322713
183142894031428941GA73GENIChomozygous110322715
183143010431430105TG43GENIChomozygous110322717
183143019131430192AG47GENIChomozygous110322719
183142266931422670TG14GENICheterozygous119567322
183142267331422674TG15GENICheterozygous119567323