chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71129705011297051CT25GENIChomozygous116003491
71129731711297318AT39GENIChomozygous115568185
71129811911298120GA22GENIChomozygous115568186
71129902411299025AC28GENIChomozygous115568187
71129907511299076TC28GENIChomozygous115568188
71129989111299892AG21GENIChomozygous115568189
71130021711300218TC19GENIChomozygous115568190
71130023311300234GA18GENIChomozygous115568191
71130139811301399AT31GENIChomozygous115568192
71130146911301470AG24GENIChomozygous115568193
71130250811302509GA21GENIChomozygous115568195
71130266611302667TC14GENIChomozygous115568196
71130293611302937CT20GENIChomozygous115568198
71130406711304068AC16GENIChomozygous115568200
71130460911304610TC15GENIChomozygous115568201
71130688211306883AG27GENIChomozygous115568205
71130874011308741GA20GENIChomozygous115568206
71131000911310010TC21GENIChomozygous115568207
71131184411311845TC22GENIChomozygous115568208
71131187111311872GA25GENIChomozygous115568209
71131237711312378GA24GENIChomozygous115568210
71131431411314315AC20GENIChomozygous115568211
71131435811314359AG23GENIChomozygous115568212
71131449211314493CT31GENIChomozygous115568213
71131136511311365G16GENIChomozygous133170259
71130042611300427TC12GENICheterozygous118275746
71130042711300428TC12GENICheterozygous118473957
71130086911300869G13GENIChomozygous128435318
71130094511300948AAA22GENIChomozygous128435319
71130535011305474CTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTCCAGCTCTCTTTTTCTTTTTCTTTTTCTTTTTTTTTTTTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTG3GENIChomozygous128435320
71130851111308511C17GENIChomozygous128435321
71130871911308719AATGTCATT19GENIChomozygous128435322
71131242211312422CA12GENIChomozygous128435323