chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71291259612912597TG18GENICpossibly homozygous53792170
71291400312914004GA18GENIChomozygous53792171
71291439112914392AC19GENIChomozygous53792172
71291457012914571TC19GENIChomozygous53792173
71291481312914814CCATG20GENIChomozygous53792174
71291495512914956CT21GENIChomozygous53792175
71291576712915768CA9GENIChomozygous53792176
71291597712915978C-24GENIChomozygous53792177
71291690312916904AG23GENIChomozygous53792178
71291705212917053CCT21GENIChomozygous53792179
71291758312917584TA18GENIChomozygous53792180
71291758712917588AC16GENIChomozygous53792181
71291806312918064TC23GENIChomozygous53792182
71291845412918455TC26GENIChomozygous53792183
71291873312918734AG15GENIChomozygous53792184
71292095612920957GA19GENIChomozygous53792185
71292161212921613TTTC10GENICpossibly homozygous53792186
71292523412925235AG12GENIChomozygous53792196
71292583612925837GA12GENIChomozygous54817967
71292643012926431TTAGTAAAGA6GENIChomozygous53792197
71292659112926592A-8GENIChomozygous54955143
71292674512926746TTA5GENIChomozygous53792198
71292812612928127TC7GENIChomozygous53792199
71292822612928227CT4GENIChomozygous53792201
71292832212928323TTA9GENIChomozygous53792202
71292845712928458AAGT4GENICheterozygous53792203
71292931412929315GA17GENIChomozygous53792204
71292955412929555GA19GENIChomozygous53792205
71292960212929603CA26GENIChomozygous53792206
71293200612932007GA6GENIChomozygous53792207