chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124707889247078893CT16GENICpossibly homozygous115397398
124707927147079272CT11GENIChomozygous115343148
124707954547079546AG14GENIChomozygous115343150
124707977547079776TC10GENIChomozygous115397400
124708012447080125GA16GENIChomozygous115397402
124708168747081688GA7GENIChomozygous115343155
124708199247081993CA8GENIChomozygous115343157
124708207447082075TC4GENIChomozygous115343159
124708222747082228AC8GENIChomozygous115397404
124708256247082563TC11GENIChomozygous115397406
124708289847082899TC15GENIChomozygous115343161
124708339947083400GA7GENIChomozygous115397408
124708350047083501CT8GENIChomozygous115343163
124708420447084205TC3GENIChomozygous115397410
124708472447084725GA17GENIChomozygous115397412
124708510447085105GA14GENIChomozygous115343165
124708524147085242CA7GENIChomozygous115397414
124708525247085253CA9GENIChomozygous115397416
124708735147087352GA9GENIChomozygous115397418
124709078247090783AG16GENIChomozygous115343179
124709118047091181AC10GENIChomozygous115397420
124709326947093270TC10GENIChomozygous115343181
124709425847094259TC8GENIChomozygous115343187