chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
159556473095564732AC14GENICheterozygous139649084
159558025995580260TA23GENICpossibly homozygous139805842
159558026195580262TA25GENICheterozygous139805843
159558026395580264TA28GENICpossibly homozygous141050098
159558025995580260T23GENICheterozygous403386824
159558664395586644GA10GENICheterozygous154903676
159558664395586644G10GENICheterozygous403386826
159558026595580266TA29GENICheterozygous141050099
159558664395586648GAGAG10GENICheterozygous141046718
159571797495717975G28GENICheterozygous403778458
159571797495717975GC28GENICheterozygous403778459
159571797695717977GC28GENICheterozygous403778460
159571797695717977G28GENICheterozygous403778461
159574706295747063A20GENICheterozygous403386869
159574706295747063AT20GENICheterozygous403386870
159575536395755364T7GENICheterozygous403778462
159575536395755364TA7GENICheterozygous403778463
159577193995771940C27GENICpossibly homozygous403386880
159577193995771940CT27GENICheterozygous403386881
159577194195771942C27GENICheterozygous403386882
159577194195771942CT27GENICpossibly homozygous403386883