chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87052289670522897AG5GENIChomozygous118149372
87052470370524704GA10GENIChomozygous118149374
87052506770525068GA8GENIChomozygous118149376
87052561970525620CT8GENIChomozygous117964626
87053090670530907TC7GENIChomozygous118149378
87053129570531296AG6GENIChomozygous117964627
87053022970530230TG5GENIChomozygous116521001
87053023770530238CT4GENIChomozygous116521003
87053264770532648AG6GENIChomozygous118149380
87053406070534061GA8GENIChomozygous118149382
87053462270534623CT12GENIChomozygous118149384
87053478370534784AG4GENIChomozygous118100631
87053700270537003TC6GENIChomozygous117964632
87053748870537489TC5GENIChomozygous117964633
87053782570537826GA6GENIChomozygous118149386
87054137570541376GA9GENIChomozygous118149388
87054157270541573CT6GENIChomozygous117964634
87054255170542552GA9GENIChomozygous118149390
87054835470548355GA4GENIChomozygous118149392
87054845670548457AG8GENIChomozygous118149394
87054897270548973TC6GENIChomozygous118149396
87054948370549484AG2GENIChomozygous117964638
87055066370550664GA4GENIChomozygous118149398
87056134870561349CT5GENIChomozygous118149402
87056209970562100AT5GENIChomozygous118149404
87056264170562642GA6GENIChomozygous118149406
87056561070565611GA8GENIChomozygous118149408
87056731170567312GT5GENIChomozygous118149410
87056851770568518AT4GENIChomozygous118149412
87057133770571338TC3GENIChomozygous117964645
87057142770571428AC3GENIChomozygous116521013
87057254570572546AG5GENIChomozygous117964647