chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71006754410067545AG44GENIChomozygous138000991
71006782910067830GA47GENIChomozygous138000992
71006867410068675CT47GENIChomozygous138000993
71006886110068862AC51GENIChomozygous138000994
71006970210069703CG64GENIChomozygous138000995
71007148710071487CATCCACCCACC4GENIChomozygous137934950
71007168710071688TC1GENIChomozygous138000996
71007309010073091CG48GENIChomozygous138000997
71007332010073321GA58GENIChomozygous138000998
71007363510073636TC53GENIChomozygous138000999
71007410310074104GA54GENIChomozygous138001000
71007579610075796A47GENICpossibly homozygous137934951
71007664410076645GA33GENIChomozygous138001001
71007692510076926GA43GENIChomozygous138001002
71007738810077389TA60GENIChomozygous138001003
71007818910078190CT42GENIChomozygous138001004
71007829810078298CGG16GENIChomozygous137934952
71007893810078939AT40GENICpossibly homozygous138001005
71008148610081487GA65GENIChomozygous138001006
71008344310083444CT52GENIChomozygous138001007
71008405010084051CT60GENIChomozygous138001008
71008484510084846CA4GENICheterozygous138001009
71008553210085533TC25GENIChomozygous138001010
71008560310085604TC33GENIChomozygous138001011
71008565210085653AC49GENIChomozygous138001012
71008719210087193AG63GENIChomozygous138001013
71008727010087271AC54GENIChomozygous138001014
71008729210087293GA61GENIChomozygous138001015
71008768510087685AG64GENIChomozygous137934953
71008833910088340AG55GENIChomozygous138001016
71008855010088551CT55GENIChomozygous138001017
71007153710071538C7GENICheterozygous403199744
71007153710071538CT7GENIChomozygous154426851
71007154110071542TC7GENIChomozygous154426852
71007154110071542T7GENICheterozygous403199745