chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103003648930036490TC25GENIChomozygous116542167
103003742930037430AC26GENIChomozygous116751949
103003776430037765AT27GENIChomozygous116542169
103003836430038365AC12GENIChomozygous116542175
103003852530038526CT17GENIChomozygous116751951
103003912130039122GA18GENIChomozygous116751953
103003920230039203TC21GENIChomozygous116542181
103003931630039317AG21GENIChomozygous116542183
103004010430040105GA29GENIChomozygous116751955
103004064830040649CT25GENIChomozygous116542189
103004070730040708CT25GENIChomozygous116542193
103004071230040713AG21GENIChomozygous116542195
103004171030041711TA29GENIChomozygous116751957
103004194130041942AG38GENIChomozygous116542203
103004230230042303TG28GENIChomozygous116751961
103004231230042313CT27GENIChomozygous116751963
103004278030042781GA18GENIChomozygous116751967
103004280830042809TG12GENIChomozygous116542211
103004315230043153TC22GENIChomozygous116542213
103004317030043171CT23GENIChomozygous116751969
103004342930043430AG25GENIChomozygous116542215
103004343730043438GA24GENIChomozygous116751971
103004523830045239CT33GENIChomozygous116751979
103004614930046150GA31GENIChomozygous116542221
103004640230046403GT25GENIChomozygous116542223
103004695130046952AG35GENIChomozygous116542225
103004735630047357CT26GENIChomozygous116542227
103004743630047437TC36GENIChomozygous116542229
103004786030047861GA17GENIChomozygous116542231
103004789530047896GC14GENIChomozygous116542233
103004814530048146AG16GENIChomozygous116751981
103004842930048430AG20GENIChomozygous116542235
103004869030048691GA20GENIChomozygous116542237