chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148573318985733190CT9GENIChomozygous66544752
148573366485733665CT15GENIChomozygous66986982
148573466685734667TC20GENIChomozygous66986984
148573510085735101AG16GENIChomozygous66544754
148573679185736792TC12GENIChomozygous66646697
148573755285737553CA20GENIChomozygous66986986
148574010085740100A17GENICheterozygous66986988
148574380585743806AC16GENIChomozygous66544758
148574526485745265CT11GENIChomozygous66544761
148574557385745574TC13GENIChomozygous66986990
148574822385748223T12GENIChomozygous66986992
148574827185748272CG16GENIChomozygous66544764
148574845285748453CA4GENIChomozygous66986994
148574845585748456CA3GENIChomozygous66582944
148574845685748457CA3GENIChomozygous66986996
148574875585748756AG16GENIChomozygous66544765
148574938285749383GT15GENIChomozygous66106653
148574950885749508A15GENIChomozygous66986998
148575043185750431T15GENICheterozygous66987000
148575186485751865AG10GENIChomozygous66106655
148575272285752722GG13GENIChomozygous66987002
148575347485753475GA6GENIChomozygous66987004
148575401485754015TC23GENIChomozygous66544767
148575446385754464TC19GENIChomozygous66987006
148575449285754493TC4GENIChomozygous66987008
148575465285754653CT9GENIChomozygous66987010
148575511785755118GA8GENIChomozygous66987012
148575512085755121GA9GENIChomozygous66646699
148575547485755475A14GENICheterozygous66987014
148575695185756952AG17GENIChomozygous66987016
148575793585757936CT11GENIChomozygous66544769