chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
13101187118101187119CT47GENICheterozygous133575234
13101206800101206800TGTGTTTGTATGTACATGGGTGTGTTCACATGTGTTCATGTA17GENIChomozygous129090859
13101248866101248867AG48GENIChomozygous133575235
13101258849101258850A17GENIChomozygous129090861
13101258859101258860T12GENIChomozygous129090862
13101258867101258868A12GENIChomozygous129090863
13101258871101258871C10GENICheterozygous129090864
13101259517101259518CT24GENIChomozygous115032964
13101259523101259524CT24GENIChomozygous118506056
13101259525101259527CA24GENIChomozygous129090865
13101259538101259538T30GENIChomozygous129090866
13101259570101259571G42GENIChomozygous129090867
13101259579101259580T43GENIChomozygous129090868
13101259632101259633C20GENIChomozygous129090869
13101259638101259638T18GENIChomozygous129090870
13101261481101261482AG14GENIChomozygous123794420
13101261482101261483CA14GENIChomozygous123794421
13101258871101258872GC10GENICheterozygous114905460
13101259622101259623GT23GENIChomozygous114437773
13101264071101264072C11GENIChomozygous129090871
13101264113101264113G26GENIChomozygous129090872
13101264240101264240C17GENIChomozygous129090873
13101264263101264263G10GENIChomozygous129090874
13101264297101264337AGTTTTACTGTAGAAGATTCTGGGGTTGTCCTGAGATGTG4GENIChomozygous129090875
13101264350101264352TG3GENIChomozygous130419682
13101264354101264355G3GENIChomozygous130419683
13101264731101264731T9GENIChomozygous129090876
13101270584101270587CCT16GENIChomozygous129090877
13101271911101271912T8GENIChomozygous129090878
13101271912101271913CG8GENIChomozygous114585107
13101276558101276559GT23GENIChomozygous114437777
13101277760101277761CA6GENIChomozygous118467511
13101277770101277772AT6GENIChomozygous129090880
13101277773101277773A6GENIChomozygous129090881