chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
63320411433204115AC37GENIChomozygous54337730
63320453433204535AG38GENIChomozygous54337733
63320574833205749GA46GENIChomozygous54337736
63320594333205944GA30GENIChomozygous54337739
63320608833206089GC34GENIChomozygous54337742
63320609133206092AG35GENIChomozygous55957067
63320609833206099AC37GENIChomozygous54337744
63320626533206266CT48GENIChomozygous54337747
63320630533206306AC47GENIChomozygous54337750
63320632333206326AAG---45GENIChomozygous54337753
63320634333206344CT43GENIChomozygous54337756
63320646133206462AG33GENIChomozygous54337759
63320647833206479GA32GENIChomozygous54337762
63320648733206488TG33GENIChomozygous54337765
63320656633206567GA32GENIChomozygous54337768
63320658133206582CT34GENIChomozygous54337770
63320675433206755AT43GENIChomozygous54337773
63320679433206795GA42GENIChomozygous54337776
63320683433206835AG35GENIChomozygous54337779
63320692233206923TG26GENIChomozygous54337782
63320728533207286GT37GENICpossibly homozygous54337785
63320755933207560GA37GENIChomozygous54337788
63320756233207563CT39GENIChomozygous54337791
63320757033207571GA47GENIChomozygous54337794
63320757733207578GGCTT45GENIChomozygous54337797
63320767933207680GT35GENIChomozygous54337800
63320775733207758AG25GENIChomozygous54337803
63320777733207778CT30GENIChomozygous54337806
63320787333207874GGGGAGTGGGCTCTGT41GENIChomozygous54337809
63320872533208726GA44GENIChomozygous54337812
63320897833208979GA35GENIChomozygous54337815
63320900233209003AG31GENIChomozygous54337818
63320910533209106T-23GENIChomozygous55957069
63320950033209502TG--11GENICheterozygous54337824
63320973633209737CT54GENIChomozygous54337828
63321063433210635CT53GENIChomozygous54337831
63321229133212292GA50GENIChomozygous54337834