chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2171184221711843G10GENIChomozygous130719066
X2171260621712607T18GENIChomozygous129726948
X2171529721715297T26GENIChomozygous129726949
X2172619921726199C9GENIChomozygous129726951
X2171285121712851GCTGTGT31GENIChomozygous133860904
X2172661321726614G16GENIChomozygous133860905
X2172833421728334T23GENIChomozygous133860906
X2171455621714557T9GENIChomozygous133593199
X2171507621715077GA25GENIChomozygous108372576
X2171552121715522TA22GENIChomozygous108372578
X2172080121720802CT21GENIChomozygous108238326
X2171985021719851CG17GENIChomozygous108372582
X2172625621726257CT11GENIChomozygous108372584
X2173112121731122GA18GENIChomozygous108372586
X2173827221738273GA15GENIChomozygous108372590
X2174078021740781TC23GENIChomozygous108238338
X2174534621745347T19GENIChomozygous129726955
X2174625821746258T25GENICpossibly homozygous133860907
X2174710721747108TG19GENIChomozygous108372592
X2174756521747566TC26GENIChomozygous108372594
X2174913021749131AC11GENIChomozygous108372596
X2175278521752785C27GENIChomozygous129726956
X2175280321752804G27GENIChomozygous129726957
X2175281921752820A23GENIChomozygous129726958
X2175283221752833A22GENIChomozygous129726959
X2175284821752849A21GENIChomozygous129726960
X2175285021752851C21GENIChomozygous129726961
X2175285621752858AA22GENIChomozygous129726962
X2175286621752867T24GENIChomozygous129726963
X2175286921752870C24GENIChomozygous129726964
X2175288221752882G23GENIChomozygous129726965
X2175292221752922C18GENIChomozygous129726966
X2175293321752934T14GENIChomozygous129726967
X2175295721752957C17GENIChomozygous129726968
X2175297721752977C20GENIChomozygous129726969
X2175297921752979C21GENIChomozygous129726970
X2175314321753143C18GENIChomozygous129726971
X2175315321753153A17GENIChomozygous129726972
X2175424121754241G20GENIChomozygous133860908
X2175540821755409TC25GENIChomozygous108372598
X2175494521754945C5GENIChomozygous132777024