chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35599922055999221AG35GENICheterozygous112340667
35600140856001409CT25GENICpossibly homozygous111577629
35600149256001493AG40GENIChomozygous111577630
35600164056001641TC34GENIChomozygous111577631
35600179656001797TC39GENIChomozygous111577632
35600628556006286AC16GENIChomozygous111577633
35600801256008013TG38GENIChomozygous111577634
35600813456008135TC58GENICheterozygous111577636
35600825056008251CA132GENICheterozygous112340668
35600827356008274GA158GENICheterozygous112340669
35600828056008281CG160GENICheterozygous112279075
35600836056008361GA85GENICheterozygous112340670
35600818356008184TC84GENICheterozygous111909912
35600832156008322AG128GENICheterozygous111909914
35600832956008330GT116GENICheterozygous111909915
35600823856008239CA144GENICheterozygous112231985
35600825256008253CG148GENICheterozygous112231987
35600992056009921AG13GENIChomozygous111577640
35601077856010779GA33GENICheterozygous111577641
35601401156014012GT22GENIChomozygous111577642
35601835756018358TC30GENIChomozygous111577644
35601863156018632AG39GENIChomozygous111577645
35602249256022493GA48GENIChomozygous111577646
35602254256022543AC46GENIChomozygous111577647
35602305356023054CT13GENICheterozygous111577650
35602306056023061CT11GENICheterozygous111577651
35602306356023064CT14GENICheterozygous111577652
35602316356023164GC20GENIChomozygous111577653
35602333256023333GA12GENICheterozygous111577654
35602333356023334CT12GENICheterozygous111577655
35602359456023595GC53GENICheterozygous111577657
35602376956023770CT67GENICheterozygous111577658
35602377156023772AG67GENICheterozygous111577659
35602465256024653AC31GENIChomozygous111577661
35602562656025627AG30GENICpossibly homozygous111577662
35602586456025865GA19GENIChomozygous111577663
35602704556027046CT28GENIChomozygous111909919
35603070956030710TG25GENIChomozygous111577664