chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104856969148569692GA14GENIChomozygous117391283
104857038148570382GA14GENIChomozygous117253389
104857041048570411GA16GENIChomozygous117253391
104857080348570804CT16GENIChomozygous133681341
104857158648571587AG19GENIChomozygous116879966
104857278948572790TA14GENIChomozygous133681342
104857280448572810ATACAT9GENIChomozygous133680302
104857366148573662CT25GENIChomozygous116879968
104857523748575238CG15GENIChomozygous116879972
104857415548574156TC18GENIChomozygous116879970
104857481148574812GA22GENIChomozygous117253393
104857520148575202GA18GENIChomozygous117253395
104857703448577035AG11GENIChomozygous116879978
104858011248580112AAC10GENIChomozygous133680303
104858039848580399CG20GENIChomozygous116879980
104858054048580540T17GENIChomozygous128815258
104858459948584599GTTTT14GENIChomozygous131092886