chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1242959982242959983CT18GENIChomozygous135851769
1242960234242960235G15GENIChomozygous135469569
1242963395242963396AC13GENIChomozygous135851770
1242964999242965000GC3GENIChomozygous135851771
1242966962242966963GA12GENIChomozygous135851772
1242967394242967395CT16GENIChomozygous135851773
1242968720242968721TC15GENIChomozygous135851774
1242970616242970617GA13GENIChomozygous135851775
1242971696242971708ATACACATACAC28GENIChomozygous135469570
1242972636242972637AG13GENIChomozygous135851776
1242972810242972811GA11GENIChomozygous135851777
1242973774242973775TC20GENIChomozygous135851778
1242975992242975993CA19GENIChomozygous135851779
1242978739242978740AG17GENIChomozygous135851780
1242978767242978768GA14GENIChomozygous135851781
1242978877242978878AC11GENIChomozygous135851782
1242978922242978923GC18GENIChomozygous135851783
1242979353242979353A17GENIChomozygous135469571
1242979514242979515GT18GENIChomozygous135851784
1242980124242980125CT24GENIChomozygous135851785
1242980705242980706CT12GENIChomozygous135851786
1242980858242980859A9GENIChomozygous135469572
1242983774242983775TA13GENIChomozygous135851787
1242984885242984886GA21GENIChomozygous135851788
1242985071242985072TC18GENIChomozygous135851789
1242986954242986955AG14GENIChomozygous135851790
1242987949242987950CG19GENIChomozygous135851791
1242988349242988350TC22GENIChomozygous135851792
1242989549242989550AG11GENIChomozygous135851793
1242990302242990303GA7GENIChomozygous135851794
1242991967242991968AG23GENIChomozygous135851795
1242992362242992363AG17GENIChomozygous135851796
1242978767242978768G14GENICheterozygous402983517
1242971707242971708CT28GENICheterozygous153920250
1242971707242971708C28GENIChomozygous402983516