chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
161432916814329169CT54GENIChomozygous111732878
161433207414332075GA49GENIChomozygous111732880
161433272214332723GT42GENIChomozygous111732882
161433428314334284GC56GENIChomozygous111732884
161433860014338601AT20GENICheterozygous119097267
161433931014339311CT50GENIChomozygous111732886
161433947014339471GA58GENICpossibly homozygous111732888
161433967414339675GA58GENIChomozygous111732890
161434009514340096TC53GENIChomozygous111732892
161434014714340148TC55GENIChomozygous111732894
161434073714340738AG64GENICpossibly homozygous111732896
161434103014341031GT66GENIChomozygous111732898
161434282714342828CG74GENIChomozygous111732900
161434417414344175CT61GENIChomozygous111732902
161434459814344599GA54GENIChomozygous111732904
161434467414344675AC53GENIChomozygous112052105
161434480514344806CT43GENICpossibly homozygous111732906
161434492914344930CT38GENIChomozygous111732908
161434502914345030GA49GENIChomozygous111732910
161434504714345048CT45GENIChomozygous111732912
161434515114345152AG52GENIChomozygous111732914
161434519614345197TG61GENIChomozygous111732916
161434623914346240AG48GENICpossibly homozygous111732918
161434625714346258CT51GENIChomozygous111732920
161434633014346331GA53GENIChomozygous111732922
161434728114347282AG58GENIChomozygous111732930
161434639214346393GA58GENIChomozygous111732924
161434708614347087GT50GENIChomozygous111732926
161434710214347103GC45GENIChomozygous111732928