chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101891509918915100GA29GENIChomozygous116741005
101891595318915954GA32GENIChomozygous116741006
101891622318916224CT29GENIChomozygous116741007
101891631118916312AT13GENIChomozygous116741008
101891651818916519GA14GENIChomozygous116741009
101891662818916629TG28GENIChomozygous116741010
101891708618917087TC18GENIChomozygous116504436
101891716818917169CT25GENIChomozygous116741011
101891719218917193TA25GENIChomozygous116741012
101891778018917781GA35GENIChomozygous116741013
101891786218917863GA34GENIChomozygous116741014
101891817018918171TA17GENIChomozygous116741015
101891819318918194GA16GENIChomozygous116741016
101891831818918319TG19GENIChomozygous116741017
101891831918918320TC20GENIChomozygous116741018
101891833618918337GA18GENIChomozygous116741019
101891838618918387GA15GENIChomozygous116741020
101891839018918391TC15GENIChomozygous116741021
101891841018918411AG18GENIChomozygous116741022
101891852418918525AG20GENIChomozygous116741023
101891870518918706AG26GENIChomozygous116741024
101891996118919962AG27GENIChomozygous116741025
101892032218920323GA25GENIChomozygous116741026
101892033518920336AT25GENIChomozygous116741027
101892037518920376CT19GENIChomozygous116741028
101892072618920727CT24GENIChomozygous116861404
101892090518920906TG18GENIChomozygous116741029
101892092218920923CT19GENIChomozygous116741030
101892131518921316CT34GENIChomozygous116741031
101892142118921422AG26GENIChomozygous116741032
101892149418921495AG25GENIChomozygous116741033
101892164618921647GA20GENIChomozygous116741034
101892165118921652GA20GENIChomozygous116741035
101892167818921679TC22GENIChomozygous116741036
101892182418921825GA24GENIChomozygous116741037
101892190318921904AG22GENIChomozygous116741038
101892204218922043CT29GENIChomozygous116741041
101892216118922162CT29GENIChomozygous116741042
101892230118922302TC27GENIChomozygous116504440
101892250218922503GC25GENIChomozygous116741043
101892276218922763CT18GENIChomozygous116741044