chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77434016274340162AATC61GENIChomozygous137960850
77434044374340444AG56GENIChomozygous138120529
77434369474343695GA59GENIChomozygous138120532
77434430974344310AT16GENICheterozygous144377243
77434572374345724CT48GENIChomozygous138120533
77434943274349433CT50GENIChomozygous138120535
77434977874349779CT65GENIChomozygous138120536
77435111074351111CT54GENIChomozygous144800037
77434121874341219CT62GENIChomozygous144800034
77434564774345648CT44GENIChomozygous144800035
77434719674347197CT62GENIChomozygous144800036
77435114374351144CG49GENIChomozygous138120539
77435241374352414GT57GENIChomozygous144800038
77435412774354128CT62GENIChomozygous144800039
77435624674356247CG53GENIChomozygous144800040
77435679174356792TC63GENIChomozygous138120543
77435788174357882AG55GENIChomozygous144800041
77436117274361173CT69GENIChomozygous138120546
77436338274363383CT55GENIChomozygous144800042
77436577574365776GT55GENICpossibly homozygous144377253
77436983874369839TC69GENIChomozygous144377255
77437071574370716AT52GENIChomozygous144800043
77437073274370733TC54GENIChomozygous138120552
77437106974371070CA59GENIChomozygous138120553
77437169174371692AG56GENIChomozygous144800044
77437223574372236CA65GENIChomozygous144800045
77437244474372445AG67GENIChomozygous138120554
77436394574363945A56GENIChomozygous144781964
77436227474362274T44GENIChomozygous144781963