chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121103829811038299AG23GENIChomozygous139082976
121103901311039014T19GENIChomozygous139040629
121103916811039169GA24GENIChomozygous139082978
121103990611039907GA19GENIChomozygous144919201
121104159611041596A14GENICpossibly homozygous147588937
121104335811043359GA23GENIChomozygous139082980
121104429611044296C25GENIChomozygous139040630
121104486811044869GC23GENIChomozygous139082981
121104514211045143AC30GENIChomozygous144919202
121104162211041626TGTA7GENIChomozygous144913194
121104913111049132TC20GENIChomozygous139082983
121105033411050335CT23GENIChomozygous139082984
121105050211050503AT22GENIChomozygous139082985
121105093911050940GA19GENIChomozygous139082986
121105200711052008CT20GENIChomozygous139082987
121105291811052918CTGGAACTCAAAGTTTACC26GENIChomozygous139040632
121105384111053842CT21GENIChomozygous139082990
121105587011055871CT25GENIChomozygous139082992
121105597511055976GA15GENIChomozygous139082993