chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104703100747031008TA11GENIChomozygous116773096
104703226947032270CT16GENIChomozygous116878165
104703499747034998GA16GENIChomozygous116878167
104703730747037308AT13GENIChomozygous116878169
104703844647038447TC19GENIChomozygous116587131
104704007147040072AT9GENIChomozygous116587133
104704099647040997CT27GENIChomozygous116878172
104704531847045319CA19GENIChomozygous116587135
104704623947046240CT6GENIChomozygous116878180
104705045647050457AG21GENICheterozygous116587137
104705152147051522GC21GENIChomozygous116587139
104705254147052542GA3GENICheterozygous126474734
104705278747052788TA4GENICheterozygous116587147
104705380747053808GA5GENIChomozygous116587149
104705461847054619CT19GENICpossibly homozygous116878182
104705479747054798GA7GENIChomozygous116878184
104705492447054925AG24GENIChomozygous116773104
104705525747055258CA8GENIChomozygous116587153
104705557247055573AG25GENIChomozygous116587155
104705600347056004AG10GENIChomozygous116587157
104705624347056244CT15GENIChomozygous116878186
104705640247056403TC19GENIChomozygous116878188
104705656747056568CG3GENICheterozygous126419291
104705666647056667TA7GENIChomozygous116878190
104705788547057886CT11GENIChomozygous116878192
104705790547057906AT12GENIChomozygous116587159
104705824947058250CT6GENIChomozygous117008782
104705839447058395TG16GENIChomozygous116878194
104705903247059033TC6GENIChomozygous116878196