chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71006754410067545AG52GENIChomozygous138000991
71007309010073091CG67GENIChomozygous138000997
71007332010073321GA55GENIChomozygous138000998
71007363510073636TC47GENIChomozygous138000999
71007818910078190CT60GENICpossibly homozygous138001004
71007579610075796A57GENIChomozygous137934951
71007410310074104GA49GENIChomozygous138001000
71007664410076645GA46GENIChomozygous138001001
71007692510076926GA48GENIChomozygous138001002
71007738810077389TA48GENIChomozygous138001003
71007829810078298CGG33GENICpossibly homozygous137934952
71007893810078939AT39GENIChomozygous138001005
71008148610081487GA56GENIChomozygous138001006
71008344310083444CT62GENIChomozygous138001007
71008405010084051CT73GENIChomozygous138001008
71008484510084846CA9GENICheterozygous138001009
71008553210085533TC20GENIChomozygous138001010
71008560310085604TC20GENIChomozygous138001011
71008565210085653AC48GENIChomozygous138001012
71008719210087193AG69GENIChomozygous138001013
71008727010087271AC56GENIChomozygous138001014
71008729210087293GA46GENIChomozygous138001015
71008768510087685AG51GENIChomozygous137934953
71008833910088340AG27GENIChomozygous138001016
71008855010088551CT51GENIChomozygous138001017
71008484710084848AC9GENICheterozygous403199747
71008484710084848A9GENICheterozygous403199746