chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121801919418019195GA34GENIChomozygous50089209
121802028418020285AG31GENIChomozygous50089211
121802102118021022CT17GENIChomozygous50089213
121802243418022435GA25GENIChomozygous50089215
121802304318023044CA31GENICheterozygous50089217
121802337418023375A-14GENIChomozygous50089221
121802352018023521AC26GENIChomozygous50089223
121802382518023826TTCACA14GENIChomozygous50089225
121802468318024684GGA16GENIChomozygous50089227
121802493318024934A-19GENICpossibly homozygous50089229
121802682618026828TA--17GENIChomozygous50089231
121802709218027093TTA12GENICpossibly homozygous50089233
121802724918027250GA22GENIChomozygous50089235
121802913118029132AAT33GENIChomozygous50089237
121802943618029438AA--12GENICpossibly homozygous50367592
121802945218029453AC14GENIChomozygous50089241
121803107918031080CT17GENIChomozygous50089243
121803133218031333GA25GENIChomozygous50089245
121803164618031647A-16GENIChomozygous50089247
121803280918032819TCTCTCTCTC----------12GENICheterozygous50089249
121803281118032819TCTCTCTC--------12GENICheterozygous50089251
121803437518034376TA26GENIChomozygous50089253
121803443518034436GA28GENIChomozygous50089255
121803453218034540ATATATAT--------10GENIChomozygous50535625
121803520418035205TTA7GENICpossibly homozygous50089259