chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2187772755187772756AG24GENIChomozygous110167780
2187772910187772911AG9GENIChomozygous110167781
2187772917187772918AG11GENIChomozygous110167782
2187773669187773670CT18GENIChomozygous110167785
2187776903187776904AG9GENIChomozygous110167800
2187780420187780421CA18GENIChomozygous110804008
2187780450187780451AG10GENIChomozygous110804009
2187780456187780457CT13GENIChomozygous110804010
2187780563187780564TC8GENIChomozygous110804011
2187781144187781145GA7GENIChomozygous110804012
2187781199187781200AC15GENIChomozygous110167806
2187781285187781286CT7GENIChomozygous110804013
2187782070187782071TC13GENIChomozygous110804020
2187783339187783340GA15GENIChomozygous110167810
2187783685187783686TG19GENIChomozygous110804021
2187784664187784665GC9GENIChomozygous110167811
2187784777187784778GA20GENIChomozygous110804023
2187785049187785050CA25GENIChomozygous110804024
2187785203187785204CA9GENIChomozygous110804025
2187785210187785211CT7GENIChomozygous110804026
2187785410187785411GA19GENICpossibly homozygous120378115
2187778759187778760CT14GENIChomozygous120378110
2187778980187778981GA21GENICpossibly homozygous120378111
2187783019187783020CT22GENIChomozygous120378112
2187784403187784404TC21GENIChomozygous120378113
2187784908187784909CT24GENIChomozygous120378114
2187786808187786809CT6GENIChomozygous120378116
2187785516187785517TG3GENICheterozygous125766373