chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71129731711297318AT50GENIChomozygous115568185
71129811911298120GA39GENIChomozygous115568186
71129902411299025AC28GENIChomozygous115568187
71129907511299076TC27GENIChomozygous115568188
71129989111299892AG37GENIChomozygous115568189
71130021711300218TC36GENIChomozygous115568190
71130023311300234GA31GENIChomozygous115568191
71130042711300428TC21GENICpossibly homozygous118473957
71130086911300869G15GENIChomozygous128435318
71130094511300948AAA21GENIChomozygous128435319
71130139811301399AT18GENIChomozygous115568192
71130146911301470AG20GENIChomozygous115568193
71130239111302392TA23GENIChomozygous115568194
71130250811302509GA32GENIChomozygous115568195
71130266611302667TC28GENIChomozygous115568196
71130284811302849TG25GENIChomozygous115568197
71130293611302937CT32GENIChomozygous115568198
71130353811303539GA18GENIChomozygous115568199
71130406711304068AC20GENIChomozygous115568200
71130460911304610TC19GENIChomozygous115568201
71130535011305474CTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTCCAGCTCTCTTTTTCTTTTTCTTTTTCTTTTTTTTTTTTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTG7GENIChomozygous128435320
71130688211306883AG34GENIChomozygous115568205
71130851111308511C36GENIChomozygous128435321
71130871911308719AATGTCATT41GENIChomozygous128435322
71130874011308741GA40GENIChomozygous115568206
71131000911310010TC29GENIChomozygous115568207
71131184411311845TC25GENIChomozygous115568208
71131187111311872GA29GENIChomozygous115568209
71131237711312378GA29GENIChomozygous115568210
71131242211312422CA29GENICpossibly homozygous128435323
71131431411314315AC33GENIChomozygous115568211
71131435811314359AG32GENIChomozygous115568212
71131449211314493CT39GENIChomozygous115568213