chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
465215916521592CT38GENIChomozygous112479417
465220256522026AG50GENIChomozygous112479419
465223586522359TC47GENIChomozygous112479421
465228826522883TC64GENIChomozygous112479425
465234166523417CT42GENIChomozygous112479427
465235346523535TC49GENICpossibly homozygous112479429
465244616524462GT49GENICpossibly homozygous112479431
465246326524633AG48GENIChomozygous112479433
465247326524733AG38GENIChomozygous112479435
465248466524847TC36GENIChomozygous112479437
465248926524893CT48GENIChomozygous112479439
465250986525099CT69GENIChomozygous112479441
465251046525105GA70GENIChomozygous112479443
465253196525320TC43GENIChomozygous112479445
465255156525516AG37GENIChomozygous112479447
465261266526127TC21GENIChomozygous112479450
465265026526503CT55GENIChomozygous112479452
465265736526574TC41GENIChomozygous112479454
465265936526594GA43GENIChomozygous112479456
465267196526720TC62GENICheterozygous112479458
465276076527608TA47GENIChomozygous112479466
465267576526758AG42GENICpossibly homozygous112479460
465268146526815AG37GENIChomozygous112479462
465272246527225AG28GENIChomozygous112479464
465276136527614CT85GENICheterozygous112479468
465276256527626GT84GENICheterozygous112479472
465276446527645TC80GENICheterozygous112479474
465276486527649CT77GENICheterozygous112479476
465276916527692GA57GENIChomozygous112479478
465281826528183AG68GENIChomozygous112479480
465283896528390CA49GENIChomozygous112479482
465285646528565AG32GENIChomozygous112479484
465288136528814CT54GENIChomozygous112479486
465289666528967GA43GENIChomozygous112479488
465293586529359AG58GENIChomozygous112479490
465296556529656GA20GENICpossibly homozygous112479492
465296756529676GT15GENICheterozygous112479494
465298536529854TC35GENIChomozygous112479496
465298626529863CT38GENIChomozygous112479498
465298926529893TC38GENIChomozygous112479500
465299896529990CT29GENIChomozygous112479502