chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103003454530034546TG25GENIChomozygous126379786
103003825130038252GA18GENIChomozygous116542173
103003648930036490TC15GENIChomozygous116542167
103003776430037765AT11GENIChomozygous116542169
103003796430037965GA11GENIChomozygous116542171
103003856630038567GA17GENIChomozygous116542177
103003881530038816AG16GENIChomozygous116542179
103003920230039203TC24GENIChomozygous116542181
103003931630039317AG11GENIChomozygous116542183
103003967630039677GT18GENIChomozygous116542185
103004051030040511GA13GENIChomozygous116542187
103004064830040649CT18GENIChomozygous116542189
103004068230040683GA11GENIChomozygous116542191
103004070730040708CT12GENIChomozygous116542193
103004071230040713AG15GENIChomozygous116542195
103004090230040903AG16GENIChomozygous116542197
103004093730040938AG18GENIChomozygous116542199
103004130630041307AG20GENIChomozygous116542201
103004194130041942AG10GENIChomozygous116542203
103004195730041958AG12GENIChomozygous116542205
103004208830042089TC13GENIChomozygous116542207
103004213830042139TC21GENIChomozygous116542209
103004280830042809TG15GENIChomozygous116542211
103004315230043153TC20GENIChomozygous116542213
103004342930043430AG20GENIChomozygous116542215
103004382930043830CT4GENIChomozygous117986339
103004590830045909GA31GENIChomozygous116542219
103004614930046150GA18GENIChomozygous116542221
103004640230046403GT18GENIChomozygous116542223
103004695130046952AG19GENIChomozygous116542225
103004735630047357CT16GENIChomozygous116542227
103004743630047437TC17GENIChomozygous116542229
103004786030047861GA14GENIChomozygous116542231
103004789530047896GC18GENIChomozygous116542233
103004814530048146AG17GENIChomozygous116751981
103004842930048430AG11GENIChomozygous116542235
103004869030048691GA15GENIChomozygous116542237