chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103533391535333916TA43GENIChomozygous116557586
103533656135336562TC40GENIChomozygous116557588
103533693935336940TC53GENIChomozygous116557590
103533985935339860CT37GENIChomozygous116757692
103534084835340849GA46GENICpossibly homozygous116557592
103534127935341280AG41GENIChomozygous116557596
103534499935345000GA51GENIChomozygous116757694
103534518435345185AC50GENICpossibly homozygous116924860
103534692635346927AG49GENIChomozygous116757696
103534874135348742AG46GENIChomozygous116557602
103535246035352461AG35GENIChomozygous116557604
103535567435355675CT41GENICpossibly homozygous117003838
103535706935357070CT33GENIChomozygous116557608
103535766435357665AC24GENICheterozygous116757698
103535799335357994AC33GENIChomozygous116557610
103535841935358420GA28GENIChomozygous116557612
103535919035359191AC37GENIChomozygous116557614
103536064535360646AT32GENIChomozygous116557616
103536169335361694CT43GENIChomozygous116557618
103536216935362170TG42GENIChomozygous116757700
103536469235364693GT56GENIChomozygous116757702
103536520535365206TC32GENICheterozygous116757704
103536528935365290AG34GENIChomozygous116757706
103536600235366003TA31GENIChomozygous116557622
103536662335366624TG24GENIChomozygous116557624
103536963035369631TC32GENIChomozygous116757708
103536966935369670AG30GENIChomozygous116867031
103537036535370366TC45GENIChomozygous116557626
103537078335370784GA29GENIChomozygous116557630