chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77434016274340162AATC54GENIChomozygous137960850
77434044374340444AG43GENIChomozygous138120529
77434369474343695GA56GENIChomozygous138120532
77434430974344310AT3GENICheterozygous144377243
77434572374345724CT59GENIChomozygous138120533
77434943274349433CT64GENIChomozygous138120535
77434977874349779CT74GENIChomozygous138120536
77435114374351144CG60GENIChomozygous138120539
77435412774354128CT64GENIChomozygous144800039
77434121874341219CT47GENIChomozygous144800034
77434564774345648CT62GENIChomozygous144800035
77434719674347197CT67GENIChomozygous144800036
77435111074351111CT58GENIChomozygous144800037
77435241374352414GT61GENICpossibly homozygous144800038
77435624674356247CG69GENIChomozygous144800040
77435679174356792TC54GENIChomozygous138120543
77435788174357882AG56GENIChomozygous144800041
77436117274361173CT51GENIChomozygous138120546
77436338274363383CT64GENIChomozygous144800042
77436577574365776GT66GENICpossibly homozygous144377253
77436983874369839TC53GENIChomozygous144377255
77437071574370716AT54GENIChomozygous144800043
77437073274370733TC52GENIChomozygous138120552
77437106974371070CA55GENIChomozygous138120553
77437169174371692AG49GENIChomozygous144800044
77437223574372236CA53GENIChomozygous144800045
77437244474372445AG70GENIChomozygous138120554
77436227474362274T54GENIChomozygous144781963
77436394574363945A57GENIChomozygous144781964