chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103003648930036490TC16GENIChomozygous116542167
103003742930037430AC16GENIChomozygous116751949
103003776430037765AT23GENIChomozygous116542169
103003836430038365AC10GENIChomozygous116542175
103003852530038526CT13GENIChomozygous116751951
103003912130039122GA24GENIChomozygous116751953
103003920230039203TC16GENIChomozygous116542181
103003931630039317AG27GENIChomozygous116542183
103004010430040105GA22GENIChomozygous116751955
103004064830040649CT22GENIChomozygous116542189
103004070730040708CT21GENIChomozygous116542193
103004071230040713AG21GENIChomozygous116542195
103004159230041593CT14GENIChomozygous116924227
103004171030041711TA8GENIChomozygous116751957
103004194130041942AG21GENIChomozygous116542203
103004197830041979AT13GENIChomozygous116751959
103004230230042303TG18GENIChomozygous116751961
103004231230042313CT16GENIChomozygous116751963
103004278030042781GA10GENIChomozygous116751967
103004280830042809TG14GENIChomozygous116542211
103004315230043153TC12GENIChomozygous116542213
103004317030043171CT15GENIChomozygous116751969
103004342930043430AG24GENIChomozygous116542215
103004343730043438GA22GENIChomozygous116751971
103004445330044454CT5GENIChomozygous116751973
103004523830045239CT30GENIChomozygous116751979
103004614930046150GA18GENIChomozygous116542221
103004640230046403GT14GENIChomozygous116542223
103004695130046952AG14GENIChomozygous116542225
103004735630047357CT20GENIChomozygous116542227
103004743630047437TC14GENIChomozygous116542229
103004786030047861GA17GENIChomozygous116542231
103004789530047896GC17GENIChomozygous116542233
103004814530048146AG13GENIChomozygous116751981
103004842930048430AG20GENIChomozygous116542235
103004869030048691GA15GENIChomozygous116542237