chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187772755187772756AG35GENIChomozygous110167780
2187772910187772911AG23GENIChomozygous110167781
2187772917187772918AG22GENIChomozygous110167782
2187773669187773670CT26GENIChomozygous110167785
2187776903187776904AG28GENIChomozygous110167800
2187780420187780421CA34GENIChomozygous110804008
2187780450187780451AG32GENIChomozygous110804009
2187780456187780457CT34GENIChomozygous110804010
2187780563187780564TC31GENIChomozygous110804011
2187781144187781145GA19GENIChomozygous110804012
2187781199187781200AC10GENIChomozygous110167806
2187781427187781428TA4GENIChomozygous110906244
2187782070187782071TC32GENIChomozygous110804020
2187783339187783340GA29GENIChomozygous110167810
2187783685187783686TG21GENIChomozygous110804021
2187784403187784404TC29GENIChomozygous120378113
2187778759187778760CT34GENIChomozygous120378110
2187778980187778981GA23GENIChomozygous120378111
2187783019187783020CT30GENIChomozygous120378112
2187784664187784665GC20GENIChomozygous110167811
2187784777187784778GA14GENIChomozygous110804023
2187784908187784909CT29GENIChomozygous120378114
2187785049187785050CA31GENIChomozygous110804024
2187785203187785204CA44GENIChomozygous110804025
2187785210187785211CT47GENIChomozygous110804026
2187785410187785411GA35GENIChomozygous120378115
2187786808187786809CT26GENIChomozygous120378116