chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46573672565736726GC40GENIChomozygous789276685
46573672665736727GC38GENIChomozygous789276686
46573733765737338TC36GENIChomozygous789276687
46573752565737526CT28GENICpossibly homozygous789276688
46573764065737641CT21GENIChomozygous789276689
46573794665737947AG23GENIChomozygous789276690
46573836365738364AT25GENIChomozygous789276691
46573880565738806GC41GENIChomozygous789276692
46573953165739532GA21GENIChomozygous789276693
46573971665739717GA13GENIChomozygous789276694
46574053165740532AG20GENIChomozygous789276695
46574121065741211GA24GENIChomozygous789276696
46574186465741865CT32GENIChomozygous789276697
46574189665741897AC29GENIChomozygous789276698
46574198265741983CT31GENIChomozygous789276699
46574262765742628CT26GENIChomozygous789276700
46574297065742971CT3GENIChomozygous789276701
46574318865743189TC23GENIChomozygous789276702
46574331565743316CT21GENIChomozygous789276703
46574411365744114AC19GENIChomozygous789276704
46574473465744735CG30GENIChomozygous789276705
46574474565744746TC29GENIChomozygous789276706
46574499665744997GA17GENIChomozygous789276707
46574502165745022AG18GENIChomozygous789276708
46574505865745059AT22GENIChomozygous789276709
46574553165745532AG25GENIChomozygous789276710
46574771065747711AG39GENIChomozygous789276711
46574795465747955AT27GENICpossibly homozygous789276712
46574848565748486TC35GENIChomozygous789276713
46574858365748584CT34GENIChomozygous789276714
46574957165749572GT28GENIChomozygous789276715
46574966965749670CT36GENIChomozygous789276716
46574999665749997AG34GENIChomozygous789276717
46580589765805898GC13GENICheterozygous789276718
46580599965806000CG22GENIChomozygous789276719
46580607065806071CT12GENIChomozygous789276720
46580607565806076CA15GENIChomozygous789276721
46581121065811211AG5GENIChomozygous789276722
46581122465811225AC7GENIChomozygous789276723