chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75093151750931518GA51GENICheterozygous54386901
75093179250931793AG29GENICpossibly homozygous53918515
75093195250931953CG25GENICheterozygous54386903
75093206250932063CT34GENICpossibly homozygous54386905
75093290750932908TC8GENICheterozygous53918520
75093293750932938CA27GENICheterozygous54386907
75093355950933560GT8GENICheterozygous54386911
75093358850933589CT12GENICheterozygous53918523
75093359850933599GT17GENICheterozygous53918524
75093360350933604CT15GENICheterozygous53918525
75093369350933694AT28GENICheterozygous54386913
75093396250933963CT19GENICheterozygous54386915
75093405650934057GA21GENICheterozygous53918528
75093438750934388CA19GENICheterozygous54386917
75093687150936872CT28GENICheterozygous54386929
75093707150937072CT10GENICheterozygous53918533
75093707250937073AG10GENICheterozygous53918534
75094029250940293AG29GENIChomozygous54386931