chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77434016274340162AATC36GENICpossibly homozygous137960850
77434044374340444AG41GENIChomozygous138120529
77434369474343695GA38GENIChomozygous138120532
77434572374345724CT60GENIChomozygous138120533
77434812674348127CT65GENIChomozygous138120534
77434943274349433CT34GENIChomozygous138120535
77434977874349779CT53GENIChomozygous138120536
77435064174350642CA44GENIChomozygous138120537
77435114374351144CG48GENIChomozygous138120539
77434202474342025CT39GENIChomozygous145629476
77434294974342949TTA48GENICpossibly homozygous145608742
77434718374347183A45GENIChomozygous145608743
77435463374354634CT55GENICpossibly homozygous145629477
77435662674356626AATC47GENIChomozygous145608744
77435679174356792TC53GENIChomozygous138120543
77435715774357158TA69GENIChomozygous145629478
77435779674357797GA51GENIChomozygous138120544
77435980674359807T48GENIChomozygous145608745
77436117274361173CT43GENIChomozygous138120546
77436481874364819AG46GENIChomozygous138120547
77436584374365844CT40GENIChomozygous145629479
77436621174366212TC48GENIChomozygous138120548
77436666474366665AG56GENICpossibly homozygous138120549
77436915274369153AT43GENIChomozygous138120550
77436929274369293AT48GENIChomozygous145629480
77437032674370327GA47GENIChomozygous138120551
77437073274370733TC57GENIChomozygous138120552
77437106974371070CA52GENIChomozygous138120553
77437244474372445AG60GENIChomozygous138120554