chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
860140756014075TA20GENIChomozygous128568642
860140926014092A15GENICheterozygous132409766
860183936018394T11GENIChomozygous128568643
860195926019594AG22GENIChomozygous128568644
860200296020030TC22GENIChomozygous116426197
860184766018477AC16GENIChomozygous116426194
860149816014982AG5GENIChomozygous116426192
860168306016831TC25GENIChomozygous116426193
860186496018650TG29GENIChomozygous116426195
860198226019823GC19GENIChomozygous116426196
860164286016429AT11GENIChomozygous117921919
860217646021765GA21GENIChomozygous116426198
860221066022110CACA18GENIChomozygous128568645
860228046022805AG17GENIChomozygous116426199
860231816023181AAAAAAAC9GENIChomozygous128568647
860231806023180C8GENIChomozygous128568646
860235376023538TC29GENIChomozygous116426200
860243316024332CT28GENICpossibly homozygous116426201
860309396030940CT25GENIChomozygous116426202
860310306031031CT21GENIChomozygous116426203
860312026031203TC17GENIChomozygous116426204
860318696031883TGCTAGAATTATAG17GENIChomozygous128568648
860320096032010GA21GENIChomozygous116426205
860332086033209CA26GENIChomozygous116426206
860337726033773GA27GENIChomozygous116426207
860342506034251GA27GENIChomozygous116426208
860363476036347A13GENIChomozygous128568649