chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117744886177448862AG28GENIChomozygous50893275
117744954877449549TC9GENIChomozygous50893277
117745096077450961AG30GENIChomozygous50893279
117745143977451440GA30GENIChomozygous51020355
117745183477451835TC24GENIChomozygous50893287
117745222377452224TTG24GENIChomozygous51020356
117745240977452410TTA27GENIChomozygous50893289
117745258577452586TA18GENIChomozygous51020357
117745296977452971TG--14GENIChomozygous51020358
117745320977453210A-22GENIChomozygous51170145
117745330977453310GC22GENIChomozygous50893299
117745396477453965TTAGCA16GENIChomozygous50893303
117745396577453966TA17GENIChomozygous51190049
117745396877453969T-17GENIChomozygous50893305
117745398977453990AATG4GENICheterozygous51190050
117745520577455206AG29GENIChomozygous50893307
117745549577455496CCTCT25GENIChomozygous50893311
117745553477455535T-26GENIChomozygous50893313
117745585877455859AG21GENIChomozygous50893315
117745585977455860AC21GENIChomozygous50893317
117745634377456344TA18GENIChomozygous51020359
117745634677456347AG18GENIChomozygous50893319
117745637377456374A-18GENIChomozygous51020360
117745643977456440TC17GENIChomozygous51020361
117745646677456467TC15GENIChomozygous51020362
117745654177456542GA24GENIChomozygous50893321
117745692177456922AATTTT13GENIChomozygous51020363
117745390277453903A-14GENIChomozygous50966484