chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71129731711297318AT40GENIChomozygous115568185
71129811911298120GA47GENIChomozygous115568186
71129902411299025AC39GENIChomozygous115568187
71129907511299076TC34GENIChomozygous115568188
71129989111299892AG43GENIChomozygous115568189
71130021711300218TC39GENIChomozygous115568190
71130023311300234GA40GENIChomozygous115568191
71130139811301399AT48GENIChomozygous115568192
71130146911301470AG47GENIChomozygous115568193
71130239111302392TA47GENIChomozygous115568194
71130250811302509GA33GENIChomozygous115568195
71130266611302667TC36GENIChomozygous115568196
71130284811302849TG21GENIChomozygous115568197
71130293611302937CT34GENIChomozygous115568198
71130353811303539GA32GENIChomozygous115568199
71130406711304068AC27GENIChomozygous115568200
71130460911304610TC18GENIChomozygous115568201
71130042611300427TC20GENICheterozygous118275746
71130042711300428TC20GENICheterozygous118473957
71130563411305635GC4GENIChomozygous115568204
71130688211306883AG44GENICpossibly homozygous115568205
71131000911310010TC42GENIChomozygous115568207
71130086911300869G28GENIChomozygous128435318
71130094511300948AAA35GENIChomozygous128435319
71130535011305474CTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCCCTCCAGCTCTCTTTTTCTTTTTCTTTTTCTTTTTTTTTTTTTCTTTTTTTCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTG4GENIChomozygous128435320
71130851111308511C38GENIChomozygous128435321
71130871911308719AATGTCATT41GENIChomozygous128435322
71130874011308741GA39GENIChomozygous115568206
71131184411311845TC28GENIChomozygous115568208
71131187111311872GA24GENIChomozygous115568209
71131237711312378GA40GENIChomozygous115568210
71131242211312422CA35GENICpossibly homozygous128435323
71131431411314315AC22GENIChomozygous115568211
71131435811314359AG24GENIChomozygous115568212
71131449211314493CT47GENIChomozygous115568213