chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141761607817616079AG22GENIChomozygous800233193
141761639017616391CT31GENIChomozygous800233194
141761847117618472TA19GENIChomozygous800233195
141762138217621383TC18GENIChomozygous800233196
141762256517622566TA25GENIChomozygous800233197
141762305917623060TC27GENIChomozygous800233198
141762436417624365CT35GENIChomozygous800233199
141762439017624391TC44GENIChomozygous800233200
141762588517625886AG27GENIChomozygous800233201
141762709017627091CA24GENIChomozygous800233202
141762915917629160GT29GENIChomozygous800233203
141762981017629811AG21GENIChomozygous800233204
141763140917631410CT29GENIChomozygous800233205