chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2171195121711952G26GENIChomozygous133353822
X2171455621714557T17GENICheterozygous133593199
X2171529721715297T27GENIChomozygous129726949
X2171665921716660TC22GENIChomozygous108700981
X2171949121719491CT16GENIChomozygous133353823
X2171955721719558TC19GENIChomozygous108372580
X2172620421726205CT12GENIChomozygous108700985
X2172080121720802CT32GENIChomozygous108238326
X2172469921724700GA38GENIChomozygous108544702
X2172732221727323CT27GENIChomozygous108544704
X2173433921734340AT30GENIChomozygous108544706
X2173852021738521CT24GENIChomozygous108544708
X2174078021740781TC36GENIChomozygous108238338
X2174718221747183AG35GENIChomozygous108544710
X2175070121750702CT25GENIChomozygous108544712
X2175278521752785C37GENIChomozygous129726956
X2175280321752804G29GENIChomozygous129726957
X2175281921752820A27GENIChomozygous129726958
X2175283221752833A27GENIChomozygous129726959
X2175284821752849A28GENIChomozygous129726960
X2175285021752851C28GENIChomozygous129726961
X2175285621752858AA26GENIChomozygous129726962
X2175286621752867T25GENIChomozygous129726963
X2175286921752870C24GENIChomozygous129726964
X2175288221752882G23GENIChomozygous129726965
X2175292221752922C28GENIChomozygous129726966
X2175293321752934T26GENIChomozygous129726967
X2175295721752957C29GENIChomozygous129726968
X2175297721752977C32GENIChomozygous129726969
X2175297921752979C33GENIChomozygous129726970
X2175314321753143C38GENIChomozygous129726971
X2175315321753153A42GENIChomozygous129726972
X2175376321753764A23GENICpossibly homozygous133353824
X2175559321755594TC15GENIChomozygous108544714