chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104703100747031008TA14GENIChomozygous116773096
104703226947032270CT20GENIChomozygous116878165
104703499747034998GA21GENIChomozygous116878167
104703730747037308AT19GENIChomozygous116878169
104703844647038447TC16GENIChomozygous116587131
104704007147040072AT13GENIChomozygous116587133
104704099647040997CT25GENIChomozygous116878172
104704531847045319CA18GENIChomozygous116587135
104704623947046240CT13GENIChomozygous116878180
104705045647050457AG23GENIChomozygous116587137
104705152147051522GC17GENIChomozygous116587139
104705278747052788TA4GENIChomozygous116587147
104705380747053808GA13GENICheterozygous116587149
104705461847054619CT17GENICpossibly homozygous116878182
104705479747054798GA13GENIChomozygous116878184
104705492447054925AG19GENIChomozygous116773104
104705525747055258CA15GENIChomozygous116587153
104705557247055573AG29GENIChomozygous116587155
104705600347056004AG8GENIChomozygous116587157
104705624347056244CT15GENIChomozygous116878186
104705640247056403TC13GENICheterozygous116878188
104705666647056667TA17GENIChomozygous116878190
104705681447056815CG5GENICheterozygous117218297
104705788547057886CT18GENIChomozygous116878192
104705790547057906AT17GENIChomozygous116587159
104705824947058250CT9GENIChomozygous117008782
104705839447058395TG23GENIChomozygous116878194
104705655147056552CG6GENICheterozygous126381952