chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
65920423459204235TC33GENICheterozygous927160747
65920803259208033TG52GENICheterozygous927160748
65921115759211158CT22GENICheterozygous927160749
65921141159211412TC40GENICheterozygous927160750
65921151259211513TC22GENICheterozygous927160751
65921175759211758AG17GENICheterozygous927160752
65921722259217223TC31GENICheterozygous927160753
65922144759221448AAT35GENICheterozygous927225544
65922144859221449CT31GENICheterozygous927160754
65922145659221457CA31GENICheterozygous927160755
65922425059224251CT17GENICheterozygous927160756
65922585659225857TC26GENICheterozygous927160757
65922625559226256AT9GENICheterozygous927160758
65922625759226258CT9GENICheterozygous927160759
65922625859226259AG9GENICheterozygous927160760
65922626059226261AAT9GENICheterozygous927225545
65922628159226282TA22GENICheterozygous927160761
65922644659226447CT52GENICheterozygous927160762
65922655059226551GT38GENICheterozygous927160763
65923689559236896CCTTAAGTATCCT22GENICheterozygous927225546
65923690459236905CT18GENICheterozygous927160764
65925917259259173CT29GENICheterozygous927160765
65925947259259473GA47GENICheterozygous927160766
65926363959263640AG32GENICheterozygous927160767
65926364459263645GA32GENICheterozygous927160768
65926552659265527AC30GENICheterozygous927160769
65926974759269748CA16GENICheterozygous927160770
65927075959270760CT23GENICheterozygous927160771
65927098259270983TTC86GENICheterozygous927225547