chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124072913740729138CT16GENIChomozygous50452357
124072915440729155CT14GENIChomozygous50452358
124073032140730322AG8GENIChomozygous50452360
124073098940730990TC14GENIChomozygous50452361
124073106640731067GA14GENIChomozygous50452362
124073138740731388TC16GENIChomozygous50452363
124073154740731548CT12GENIChomozygous50452364
124073274440732745CA12GENIChomozygous50543745
124073275440732755AAG15GENIChomozygous50452365
124073276640732767AAAG15GENIChomozygous50452366
124073289240732893CT20GENIChomozygous50452367
124073416540734166CT14GENIChomozygous50452369
124073441740734418CT15GENIChomozygous50452370
124073470940734710TC12GENIChomozygous50452371
124073479240734793AACC4GENIChomozygous50452372
124073479740734798TC5GENIChomozygous50512461
124073488040734881GA6GENIChomozygous50452373
124073494240734946AAAA----8GENIChomozygous50452374
124073528740735288CCTTTTT7GENIChomozygous50452375
124073531940735320CT9GENIChomozygous50452377
124073551240735513TC11GENIChomozygous50204502
124073570540735733ATCTATCTATCTATCTATCTATCTATCT----------------------------11GENIChomozygous50512463
124073590440735905TC8GENIChomozygous50204503
124073666440736665GA13GENIChomozygous50422959
124073724340737244GT8GENIChomozygous50204506
124073730840737309CCAAAAAA3GENICheterozygous50543747
124073748840737489CA10GENIChomozygous50422961
124073860340738605CA--9GENICheterozygous50543748
124073930240739303GGAAA9GENIChomozygous50571771
124073934640739348TT--7GENICpossibly homozygous50422962
124073934740739348T-7GENICheterozygous50422963
124073954140739542CCT11GENIChomozygous50452380
124073985140739852TA19GENIChomozygous50422964
124073996140739962CT11GENIChomozygous50204531
124074034540740346GA17GENIChomozygous50422965