chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7129368103129368104GA18GENIChomozygous54108596
7129370676129370677CT22GENIChomozygous54108597
7129372684129372685CT13GENIChomozygous54108601
7129373120129373121AG12GENIChomozygous54108602
7129374732129374733TTG10GENIChomozygous54108603
7129376995129376996CT23GENIChomozygous54108604
7129377368129377369AC16GENIChomozygous54108607
7129378475129378476TC11GENIChomozygous54108609
7129381122129381123CA20GENIChomozygous54108610
7129385610129385611A-7GENIChomozygous54922249
7129385612129385680GCTCCACTCTAGCAAGAATCATTCCTTTCAAAAAGCTGGCATACGTCAGTCCCCTCCAGCCAGGGCCA--------------------------------------------------------------------8GENIChomozygous54922251
7129386736129386737GT15GENIChomozygous54108614
7129387324129387325AG17GENIChomozygous54108615
7129389212129389213CT17GENIChomozygous54108616
7129389400129389401GA19GENIChomozygous54108617
7129390118129390119GA10GENIChomozygous54108618
7129390127129390128GA12GENIChomozygous54108619
7129390144129390145CT14GENIChomozygous54108620
7129390165129390166CT10GENIChomozygous54108621
7129390246129390247GA17GENIChomozygous54108622
7129390258129390259CG15GENIChomozygous54108623
7129390260129390261CT15GENIChomozygous54108624
7129390264129390265TTG17GENIChomozygous54108625
7129390432129390433CG20GENIChomozygous54108627
7129390526129390527CA16GENIChomozygous54108628
7129391261129391286CCAAGCCAGCCTGACCCACGTGCAG-------------------------8GENIChomozygous54108629
7129391444129391445GA16GENIChomozygous54108630
7129391730129391731AG29GENIChomozygous54108631
7129394496129394498AC--15GENIChomozygous54108633
7129394651129394652TC17GENIChomozygous54108634
7129401175129401176TC10GENIChomozygous54108636
7129407173129407174AAACG16GENIChomozygous54108643
7129408231129408232AG28GENIChomozygous54108646
7129411019129411020CG16GENIChomozygous54108647
7129374733129374734CG10GENIChomozygous55009967