chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1468013346801335CT22GENIChomozygous113571982
1468013386801339CT23GENIChomozygous113571983
1468014176801441CTCCGTAGTCGAACCTTAGCCGTT15GENIChomozygous131141488
1468015076801508TG18GENIChomozygous113571984
1468015126801513TC18GENIChomozygous113571985
1468015576801558AG16GENIChomozygous113571987
1468016206801621GA19GENIChomozygous113571988
1468016836801684GA24GENIChomozygous113571989
1468016846801685GC24GENIChomozygous113571990
1468016896801690GC24GENIChomozygous113571991
1468017136801714T21GENIChomozygous131141489
1468017476801748TC25GENIChomozygous113571992
1468018606801861AG24GENIChomozygous113715621
1468018916801892CT17GENIChomozygous113571993
1468019046801905CT14GENIChomozygous113571994
1468019386801939CA10GENIChomozygous113715623
1468019766801977GA5GENIChomozygous113715625
1468043236804324GA20GENIChomozygous113571996
1468037486803749CA31GENIChomozygous113323828
1468055466805547AG28GENIChomozygous113323831
1468056676805668AC17GENIChomozygous113571997
1468057906805791AG23GENIChomozygous113571998
1468058066805807AG23GENIChomozygous113571999
1468058086805809AG23GENIChomozygous113572000
1468064816806482TG22GENIChomozygous113572001
1468071966807197TC28GENIChomozygous113323834
1468075436807544CT29GENIChomozygous113572002
1468079436807944GA18GENIChomozygous113572003
1468086986808699TA30GENIChomozygous113323836
1468088716808872TA26GENIChomozygous113323837
1468103196810320GA24GENIChomozygous113323838
1468105336810534GT27GENIChomozygous113323839
1468045096804511GA27GENIChomozygous129120903
1468125466812547GA6GENIChomozygous118674250
1468137626813763AT29GENICpossibly homozygous113323840