chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101205215101205219CTAG23GENIChomozygous135352695
13101206800101206800TGTGTTTGTATGTACATGGGTGTGTTCACATGTGTTCATGTA9GENIChomozygous129090859
13101208897101208898CT21GENIChomozygous126157769
13101258849101258850A9GENIChomozygous129090861
13101258859101258860T8GENIChomozygous129090862
13101258867101258868A7GENIChomozygous129090863
13101258871101258871C7GENIChomozygous129090864
13101259517101259518CT12GENIChomozygous115032964
13101259523101259524CT11GENIChomozygous118506056
13101259525101259527CA11GENIChomozygous129090865
13101259538101259538T12GENIChomozygous129090866
13101259570101259571G14GENIChomozygous129090867
13101259579101259580T16GENIChomozygous129090868
13101259632101259633C1GENIChomozygous129090869
13101259638101259638T1GENIChomozygous129090870
13101261481101261482AG5GENIChomozygous123794420
13101261482101261483CA6GENIChomozygous123794421
13101262853101262853G1GENIChomozygous134959278
13101264071101264072C9GENIChomozygous129090871
13101264113101264113G10GENIChomozygous129090872
13101264240101264240C8GENIChomozygous129090873
13101264263101264263G8GENIChomozygous129090874
13101264297101264337AGTTTTACTGTAGAAGATTCTGGGGTTGTCCTGAGATGTG2GENIChomozygous129090875
13101264731101264731T5GENIChomozygous129090876
13101270584101270587CCT11GENIChomozygous129090877
13101271911101271912T3GENIChomozygous129090878
13101276570101276693ATATCGTATTCGAGATCTTTGATCGCGTCATCGGGCGTGTCATCTTCTTCATCATCCTCCCCCTCCTCTTCCTCCTCCTCCTCCTCCTCCTCCTCCTTCTGGTTTGATATTCTTTTTCATTTC17GENICheterozygous130585850
13101259622101259623GT1GENIChomozygous114437773
13101276558101276559GT14GENIChomozygous114437777
13101271912101271913CG3GENIChomozygous114585107
13101277760101277761CA1GENIChomozygous118467511
13101277770101277772AT2GENIChomozygous129090880
13101277773101277773A2GENIChomozygous129090881