chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
148573318985733190CT9GENIChomozygous66544752
148573366485733665CT23GENIChomozygous66986982
148573466685734667TC20GENIChomozygous66986984
148573510085735101AG20GENIChomozygous66544754
148573656185736562TA10GENIChomozygous67090763
148573755285737553CA23GENIChomozygous66986986
148574380585743806AC14GENIChomozygous66544758
148574526485745265CT6GENIChomozygous66544761
148574557385745574TC14GENIChomozygous66986990
148574827185748272CG15GENIChomozygous66544764
148574845285748453CA7GENIChomozygous66986994
148574875585748756AG22GENIChomozygous66544765
148573679185736792TC19GENIChomozygous66646697
148573903685739036A9GENICheterozygous67300103
148574010085740100A25GENICheterozygous67300104
148574161385741614AT5GENIChomozygous67300105
148574822385748223T24GENICheterozygous67300106
148574950885749508A27GENICheterozygous67300107
148575043185750431T16GENICheterozygous67300108
148574938285749383GT30GENIChomozygous66106653
148575099085750990A9GENICheterozygous67300109
148575186485751865AG12GENIChomozygous66106655
148575272285752722GG16GENICheterozygous67300110
148575347485753475GA11GENIChomozygous66987004
148575401485754015TC24GENICheterozygous66544767
148575446385754464TC22GENIChomozygous66987006
148575451085754511TC6GENIChomozygous67090775
148575465285754653CT16GENIChomozygous66987010
148575511785755118GA5GENIChomozygous66987012
148575512085755121GA5GENIChomozygous66646699
148575547485755475A21GENICheterozygous66987014
148575633585756336CT4GENIChomozygous67166495
148575695185756952AG34GENIChomozygous66987016
148575793585757936CT11GENIChomozygous66544769