chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533391535333916TA16GENIChomozygous116557586
103533656135336562TC41GENIChomozygous116557588
103533693935336940TC40GENIChomozygous116557590
103534084835340849GA56GENICpossibly homozygous116557592
103534127935341280AG51GENIChomozygous116557596
103534518435345185AC37GENIChomozygous116924860
103534874135348742AG64GENIChomozygous116557602
103535246035352461AG62GENIChomozygous116557604
103535706935357070CT33GENIChomozygous116557608
103535799335357994AC45GENIChomozygous116557610
103535841935358420GA39GENIChomozygous116557612
103535919035359191AC53GENIChomozygous116557614
103536064535360646AT67GENIChomozygous116557616
103536169335361694CT49GENIChomozygous116557618
103536216935362170TG51GENICpossibly homozygous116757700
103533985935339860CT39GENIChomozygous116757692
103534499935345000GA33GENIChomozygous116757694
103534692635346927AG45GENIChomozygous116757696
103535766435357665AC50GENICheterozygous116757698
103535567435355675CT40GENICpossibly homozygous117003838
103536469235364693GT39GENIChomozygous116757702
103536520535365206TC37GENICpossibly homozygous116757704
103536528935365290AG33GENIChomozygous116757706
103536600235366003TA52GENIChomozygous116557622
103536662335366624TG64GENIChomozygous116557624
103536963035369631TC45GENIChomozygous116757708
103536966935369670AG46GENICpossibly homozygous116867031
103537036535370366TC52GENIChomozygous116557626
103537078335370784GA53GENIChomozygous116557630