chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1196999057196999058TA31GENIChomozygous108492937
1197000274197000275AG29GENIChomozygous108492945
1197001476197001477AG25GENIChomozygous108492949
1197001924197001925AG23GENIChomozygous108492951
1197001958197001959AT23GENIChomozygous108492953
1197002023197002024AT20GENIChomozygous108492955
1197002996197002997GA23GENIChomozygous108492957
1197004534197004535TC23GENIChomozygous108492959
1197004627197004628GA23GENIChomozygous108492961
1197004856197004857GT31GENIChomozygous108492963
1197005020197005021GA17GENIChomozygous108492965
1197005922197005923AG26GENIChomozygous108492969
1197006199197006200TC22GENIChomozygous108492971
1197006389197006390GT29GENIChomozygous108492973
1197006934197006935CT24GENIChomozygous108492975
1197007812197007813CT31GENIChomozygous108492977
1197008143197008144TC16GENIChomozygous108492979
1197009133197009134CG34GENIChomozygous108492981
1197009134197009135GA34GENIChomozygous108492983
1197009209197009210CT25GENIChomozygous108492985
1197009641197009642TA25GENIChomozygous108492987
1197010059197010060GA12GENIChomozygous108492989
1197011820197011821GC28GENIChomozygous108492991
1197012444197012445AG22GENIChomozygous108492993
1197012822197012823AG19GENIChomozygous120475349
1197012824197012825GA21GENIChomozygous120475350
1197013967197013968TC39GENIChomozygous108492995
1197014855197014856CT26GENIChomozygous108492997
1197015048197015049AG38GENIChomozygous108492999
1197016871197016872TC37GENIChomozygous108493001
1197018374197018375CG21GENIChomozygous108493003
1197018547197018548TA29GENIChomozygous108493005
1197018834197018835TC26GENIChomozygous108493007
1197018910197018911CT21GENIChomozygous108493009
1197021560197021561CG23GENIChomozygous108493011
1197021868197021869GT30GENIChomozygous108493013
1197022147197022148CG21GENIChomozygous108493015
1197022542197022543AG19GENIChomozygous108493017
1197022563197022564CT18GENIChomozygous108493019
1197023106197023107CT30GENIChomozygous108493021