chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6127872197127872198GA26GENIChomozygous118734985
6127872973127872974GA27GENIChomozygous118734986
6127873127127873128AC21GENIChomozygous114984172
6127880355127880356CA20GENIChomozygous118734987
6127880576127880577GT29GENIChomozygous118734988
6127880580127880581TA27GENIChomozygous118734989
6127880702127880703TC24GENIChomozygous118734990
6127880732127880733TC31GENIChomozygous118734991
6127880750127880751AG27GENIChomozygous118734992
6127880758127880759TC27GENIChomozygous118734993
6127880775127880776GA25GENIChomozygous118734994
6127880776127880777CT24GENIChomozygous118734995
6127880876127880877AG23GENIChomozygous118734996
6127881408127881409CT28GENIChomozygous118734997
6127882053127882054AG20GENIChomozygous114984176
6127882240127882241GA22GENIChomozygous114984177
6127882828127882829CT32GENIChomozygous118734998
6127884185127884186TC24GENIChomozygous118734999
6127885675127885676GA26GENIChomozygous118735000
6127885876127885877TC25GENIChomozygous118735001
6127886074127886075TC26GENIChomozygous118735002
6127886617127886618TC22GENIChomozygous118735003
6127886643127886644TC18GENIChomozygous114984180
6127886952127886953AT21GENIChomozygous118735004
6127887080127887081GT36GENIChomozygous118735005
6127887705127887706GT34GENIChomozygous118735006
6127887886127887887CT21GENIChomozygous118735007
6127888141127888142GT25GENIChomozygous118735008
6127888150127888151AT22GENIChomozygous118735009