chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121801919418019195GA18GENIChomozygous50089209
121802028418020285AG21GENIChomozygous50089211
121802102118021022CT18GENIChomozygous50089213
121802243418022435GA30GENIChomozygous50089215
121802304318023044CA9GENIChomozygous50089217
121802337418023375A-14GENIChomozygous50089221
121802352018023521AC23GENIChomozygous50089223
121802382518023826TTCACA16GENIChomozygous50089225
121802468318024684GGA19GENICpossibly homozygous50089227
121802493318024934A-11GENICpossibly homozygous50089229
121802682618026828TA--14GENIChomozygous50089231
121802709218027093TTA7GENICheterozygous50089233
121802709318027094A-7GENICheterozygous50535623
121802724918027250GA16GENIChomozygous50089235
121802913118029132AAT17GENIChomozygous50089237
121802943618029438AA--10GENIChomozygous50367592
121802945218029453AC15GENIChomozygous50089241
121803107918031080CT17GENIChomozygous50089243
121803133218031333GA5GENIChomozygous50089245
121803164618031647A-26GENIChomozygous50089247
121803280918032819TCTCTCTCTC----------14GENICheterozygous50089249
121803281118032819TCTCTCTC--------14GENICpossibly homozygous50089251
121803443518034436GA3GENIChomozygous50089255
121803453218034540ATATATAT--------2GENIChomozygous50535625
121803520418035205TTA16GENIChomozygous50089259