chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
465215916521592CT25GENIChomozygous112479417
465220256522026AG41GENIChomozygous112479419
465223586522359TC22GENIChomozygous112479421
465228826522883TC29GENIChomozygous112479425
465234166523417CT17GENIChomozygous112479427
465235346523535TC11GENIChomozygous112479429
465244616524462GT23GENIChomozygous112479431
465246326524633AG18GENIChomozygous112479433
465247326524733AG19GENIChomozygous112479435
465248466524847TC21GENIChomozygous112479437
465248926524893CT19GENIChomozygous112479439
465250986525099CT25GENIChomozygous112479441
465251046525105GA26GENIChomozygous112479443
465253196525320TC17GENIChomozygous112479445
465255156525516AG23GENICpossibly homozygous112479447
465265026526503CT19GENIChomozygous112479452
465265736526574TC20GENIChomozygous112479454
465265936526594GA19GENIChomozygous112479456
465272246527225AG22GENIChomozygous112479464
465276916527692GA21GENIChomozygous112479478
465281826528183AG22GENIChomozygous112479480
465283896528390CA15GENIChomozygous112479482
465285646528565AG18GENIChomozygous112479484
465288136528814CT25GENIChomozygous112479486
465288486528849CT24GENIChomozygous119272842
465289666528967GA18GENIChomozygous112479488
465293586529359AG32GENIChomozygous112479490
465296756529676GT3GENIChomozygous112479494
465298536529854TC8GENIChomozygous112479496
465298626529863CT9GENIChomozygous112479498
465298926529893TC18GENIChomozygous112479500
465299896529990CT12GENIChomozygous112479502