chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106325293763252938CT48GENIChomozygous147694698
106325298863252992TTTG35GENIChomozygous138687312
106325426963254270CT48GENIChomozygous138804471
106325864563258646GA44GENIChomozygous147694699
106325916363259164GT53GENICpossibly homozygous147694700
106326044363260444CT40GENIChomozygous147694701
106326116863261169TC63GENIChomozygous138804477
106326122563261226CT54GENIChomozygous138804478
106326188863261889GA50GENIChomozygous147694702
106326258163262582AG58GENIChomozygous147694703
106326273363262734TC51GENIChomozygous138804480
106326335163263352AG69GENIChomozygous138804482
106326376163263762AC48GENIChomozygous138804483
106326582563265826AG49GENIChomozygous138804489
106326821563268216CT57GENIChomozygous147694705
106326037963260379TTT29GENIChomozygous147693095
106326658063266580AG39GENIChomozygous147693096
106326672663266727TC2GENIChomozygous138804492
106326673463266735TC7GENIChomozygous138804493
106326745763267458AT57GENIChomozygous147694704
106326676263266763T10GENICheterozygous404501808
106326676263266763TC10GENIChomozygous404501809
106326675063266751TC2GENIChomozygous145215777
106326673663266736T2GENIChomozygous147750672
106326674663266747TC2GENIChomozygous147751693
106326675463266755TC2GENIChomozygous147751694
106326843163268432GC63GENIChomozygous147694706
106327123763271238TA44GENIChomozygous147694707
106327129663271297CA58GENICpossibly homozygous147694708
106327165863271659AG55GENIChomozygous138804510
106327208663272087TC39GENIChomozygous138804511
106327210663272106ACACACAAATACACACATACACACACACAATACAAAT34GENIChomozygous147693097
106327258663272587CT48GENIChomozygous147694709
106327324863273249CT36GENIChomozygous147694710