chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6107550924107550925GA59GENIChomozygous115471724
6107551212107551213GA63GENIChomozygous115471726
6107551405107551406AG14GENIChomozygous115471728
6107551446107551447CA23GENICpossibly homozygous115471730
6107551528107551529GA36GENICpossibly homozygous115471732
6107551535107551536CT39GENICpossibly homozygous115471734
6107551564107551565AC35GENIChomozygous115471736
6107551717107551718CG32GENIChomozygous115471738
6107553034107553035TA27GENIChomozygous115471740
6107553093107553094GA40GENIChomozygous115471742
6107553288107553289CT56GENIChomozygous115471744
6107553615107553616TC44GENIChomozygous115471746
6107553903107553904TC36GENIChomozygous115471748
6107554452107554453GC43GENICpossibly homozygous115471750
6107554648107554649AG41GENIChomozygous115471752
6107555072107555073AG6GENIChomozygous115504174
6107555274107555275CT30GENICheterozygous115471754
6107555363107555364AG44GENICpossibly homozygous115471756
6107556600107556601AG48GENIChomozygous115471758
6107556696107556697GA67GENIChomozygous115471760
6107557092107557093TA54GENIChomozygous115471762
6107557265107557266AG42GENIChomozygous115471764
6107557647107557648TG57GENICpossibly homozygous115471766