chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
95390630353906304CG12GENIChomozygous117341810
95390632653906327CT10GENIChomozygous117341811
95390677853906779GA36GENICpossibly homozygous117341812
95390765553907656TC19GENIChomozygous117341813
95390916453909165AG50GENIChomozygous117341814
95390920553909206GT42GENIChomozygous117341815
95391064053910641CT51GENIChomozygous117341816
95391065853910659TA55GENIChomozygous117341817
95391140753911408TA32GENICpossibly homozygous117341818
95391144753911448GA36GENIChomozygous117341819
95391315853913159TG31GENIChomozygous117341820
95391366953913670GA16GENIChomozygous117341821
95391376553913766CT41GENIChomozygous117341822
95391381053913811AG43GENIChomozygous117341823
95391430053914301CT30GENIChomozygous117341824
95391740953917410GA31GENIChomozygous117341825
95392080653920807CT48GENIChomozygous117341826
95392117753921178CA24GENIChomozygous117341827
95392513953925140GA32GENIChomozygous117341828
95393465553934656AG42GENIChomozygous117341829
95393468053934681GA44GENIChomozygous117341830
95393689153936892GA30GENIChomozygous117341831
95393925453939255TC24GENIChomozygous117341832
95394043653940437AT44GENIChomozygous117341833
95394146053941461GT37GENICheterozygous117341834
95394146353941464GT39GENICheterozygous117341835
95394147653941477TG32GENICheterozygous117341836
95394209553942096CT41GENIChomozygous117341837
95394242553942426CA56GENIChomozygous117341838
95394279353942794TC44GENIChomozygous117341839
95394461253944613GT42GENIChomozygous117341840
95394489453944895TC35GENICpossibly homozygous117341841
95394545853945459TC17GENIChomozygous117341842