chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173055723930557240CA22GENIChomozygous111317130
173055833530558336GA16GENIChomozygous111022869
173055846930558470CT23GENIChomozygous111022871
173055927230559273AG26GENIChomozygous111022873
173055942830559429AG27GENIChomozygous111022875
173055955730559558AG21GENIChomozygous111022877
173056043530560436AT41GENIChomozygous111022881
173056093730560938TC36GENIChomozygous111022884
173056110530561106CT23GENIChomozygous111022886
173056111030561111GA22GENIChomozygous111022888
173056129930561300CT26GENIChomozygous111022890
173056228430562285CG34GENICpossibly homozygous111022896
173056257330562574AC27GENIChomozygous111022898
173056263930562640AG28GENIChomozygous111022900
173056267930562680GA29GENIChomozygous111022902
173056271030562711GA34GENIChomozygous111022904
173056297430562975GA29GENIChomozygous111022908
173056298630562987GA26GENIChomozygous111022910
173056306130563062AC30GENIChomozygous111022912
173056307230563073GA29GENIChomozygous111022914
173056308930563090GA30GENIChomozygous111022916
173056325030563251TC31GENIChomozygous111022918
173056325730563258TA32GENIChomozygous111022920
173056329130563292AG27GENIChomozygous111022922
173056332330563324GA37GENIChomozygous111022924
173056339230563393AG28GENIChomozygous111022926
173056341330563414GA24GENIChomozygous111022928
173056342030563421AG23GENIChomozygous111022930
173056441930564420AC34GENICheterozygous111022940
173056776330567764AT3GENIChomozygous111022969
173056820930568210AG21GENIChomozygous111022977
173056822530568226AT20GENIChomozygous111022979
173056822630568227AC20GENIChomozygous111022981
173056859330568594GA17GENIChomozygous111317132
173056975130569752GA28GENICpossibly homozygous111317134
173057181830571819GA30GENIChomozygous111317136
173057301230573013GT30GENIChomozygous111317139
173057301330573014TA31GENIChomozygous111317141
173056438430564385AC58GENICheterozygous111189594
173056439430564395TG50GENICheterozygous111189596
173056441730564418TC33GENICheterozygous111241815