chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7143937632143937633GT45GENICheterozygous116396875
7143942010143942011GA55GENICpossibly homozygous116396876
7143942291143942292AG35GENICpossibly homozygous116396877
7143942373143942374TC39GENIChomozygous116396878
7143942641143942642AG44GENIChomozygous116396879
7143942890143942891AC45GENIChomozygous115944797
7143943180143943181CT64GENIChomozygous116396880
7143943735143943736CA24GENIChomozygous116396881
7143945583143945584AG61GENIChomozygous115944798
7143946079143946080AT49GENIChomozygous115944799
7143947046143947047CT29GENIChomozygous116396882
7143947715143947716TC29GENIChomozygous116396883
7143947910143947911GA48GENICpossibly homozygous116396884
7143948028143948029CT47GENICpossibly homozygous116396885
7143948053143948054CT42GENICpossibly homozygous116396886
7143948257143948258AG26GENIChomozygous116396887
7143948523143948524GA26GENIChomozygous116396888
7143948622143948623TC42GENIChomozygous116396889
7143949334143949335GC48GENICheterozygous115944800
7143949351143949352TC38GENIChomozygous115944801
7143949918143949919CT47GENIChomozygous116396890
7143952424143952425TC53GENIChomozygous116396891
7143955614143955615TC41GENIChomozygous115944802
7143956062143956063GA43GENIChomozygous116396892
7143956510143956511CT17GENIChomozygous116396893