chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187772755187772756AG23GENIChomozygous110167780
2187772910187772911AG32GENIChomozygous110167781
2187772917187772918AG29GENIChomozygous110167782
2187773669187773670CT26GENIChomozygous110167785
2187776903187776904AG24GENICpossibly homozygous110167800
2187780420187780421CA31GENICpossibly homozygous110804008
2187780450187780451AG36GENIChomozygous110804009
2187780456187780457CT38GENIChomozygous110804010
2187780563187780564TC24GENIChomozygous110804011
2187781144187781145GA15GENICpossibly homozygous110804012
2187781199187781200AC20GENIChomozygous110167806
2187781285187781286CT12GENIChomozygous110804013
2187782070187782071TC25GENICpossibly homozygous110804020
2187783339187783340GA15GENIChomozygous110167810
2187783685187783686TG26GENICpossibly homozygous110804021
2187784664187784665GC19GENIChomozygous110167811
2187784777187784778GA23GENICpossibly homozygous110804023
2187784908187784909CT30GENICpossibly homozygous120378114
2187778759187778760CT18GENIChomozygous120378110
2187778980187778981GA32GENICpossibly homozygous120378111
2187783019187783020CT31GENICpossibly homozygous120378112
2187784403187784404TC45GENICpossibly homozygous120378113
2187785049187785050CA38GENIChomozygous110804024
2187785203187785204CA27GENICpossibly homozygous110804025
2187785210187785211CT29GENICpossibly homozygous110804026
2187785410187785411GA15GENICpossibly homozygous120378115
2187786808187786809CT21GENICpossibly homozygous120378116