chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124707889247078893CT11GENIChomozygous115397398
124707927147079272CT23GENIChomozygous115343148
124707954547079546AG23GENIChomozygous115343150
124708012447080125GA28GENIChomozygous115397402
124708168747081688GA36GENIChomozygous115343155
124708199247081993CA27GENIChomozygous115343157
124708207447082075TC24GENIChomozygous115343159
124708256247082563TC11GENIChomozygous115397406
124708339947083400GA31GENIChomozygous115397408
124708350047083501CT16GENIChomozygous115343163
124708472447084725GA27GENIChomozygous115397412
124708510447085105GA22GENIChomozygous115343165
124708524147085242CA21GENICpossibly homozygous115397414
124708525247085253CA25GENIChomozygous115397416
124708735147087352GA22GENIChomozygous115397418
124709078247090783AG30GENIChomozygous115343179
124709326947093270TC19GENIChomozygous115343181
124709347547093476CT20GENIChomozygous115343185
124709425847094259TC18GENIChomozygous115343187