chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71006754410067545AG60GENIChomozygous138000991
71006782910067830GA57GENIChomozygous138000992
71006867410068675CT57GENIChomozygous138000993
71006886110068862AC50GENIChomozygous138000994
71006970210069703CG60GENIChomozygous138000995
71007148710071487CATCCACCCACC5GENIChomozygous137934950
71007154110071542T6GENICheterozygous403199745
71007153710071538CT6GENIChomozygous154426851
71007153710071538C6GENICheterozygous403199744
71007154110071542TC6GENIChomozygous154426852
71007168710071688TC4GENIChomozygous138000996
71007309010073091CG45GENIChomozygous138000997
71007332010073321GA54GENIChomozygous138000998
71007363510073636TC41GENIChomozygous138000999
71007410310074104GA50GENIChomozygous138001000
71007579610075796A40GENICpossibly homozygous137934951
71007664410076645GA45GENIChomozygous138001001
71007692510076926GA45GENIChomozygous138001002
71007738810077389TA54GENIChomozygous138001003
71007818910078190CT45GENIChomozygous138001004
71007829810078298CGG21GENIChomozygous137934952
71007893810078939AT58GENIChomozygous138001005
71008148610081487GA59GENIChomozygous138001006
71008344310083444CT58GENIChomozygous138001007
71008405010084051CT56GENIChomozygous138001008
71008484510084846CA9GENICheterozygous138001009
71008484710084848A10GENICheterozygous403199746
71008484710084848AC10GENICheterozygous403199747
71008553210085533TC25GENIChomozygous138001010
71008560310085604TC24GENIChomozygous138001011
71008729210087293GA56GENIChomozygous138001015
71008565210085653AC40GENIChomozygous138001012
71008719210087193AG52GENIChomozygous138001013
71008727010087271AC57GENIChomozygous138001014
71008768510087685AG46GENIChomozygous137934953
71008833910088340AG44GENIChomozygous138001016
71008855010088551CT46GENIChomozygous138001017