chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47597996275979963AG23GENIChomozygous185298678
47597998075979981GA19GENIChomozygous187141257
47598138175981382AT7GENICheterozygous187141258
47598199975982000GA17GENIChomozygous187141259
47598249375982494TG15GENIChomozygous187141260
47598386575983866AC19GENIChomozygous187141261
47598490175984902AG19GENIChomozygous185298679
47598629875986299GA21GENIChomozygous187141262
47598856475988565GA11GENIChomozygous185298680
47598913175989132GT18GENICpossibly homozygous185298681
47598979275989793CT19GENIChomozygous187141263
47599040775990408GT11GENIChomozygous187141264
47599134375991344AT13GENIChomozygous185298682
47599404175994042AG19GENIChomozygous185298683
47599600475996005AG15GENIChomozygous185298684
47599600575996006TA16GENIChomozygous185298685
47599637475996375AG17GENIChomozygous185298686
47599682975996830CT3GENIChomozygous187141265
47599698275996983GC3GENIChomozygous187141266
47599920075999201AG19GENIChomozygous187141267
47600053876000539CT20GENIChomozygous187141268
47600147476001475TA5GENIChomozygous185298687
47600147876001479TC3GENIChomozygous185298688
47600149476001495TA6GENIChomozygous185298689
47600153876001539TG13GENIChomozygous185298690
47600154076001541CT11GENIChomozygous185298691
47600160276001603AC7GENIChomozygous185298692
47600164676001647AG4GENIChomozygous187141269
47600165076001651AC5GENIChomozygous185298693