chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2114413751114413752CT52INTERGENIChomozygous59029983
2114413952114413953GA37INTERGENIChomozygous59029984
2114414701114414824GAGCAAATCTATTTTTTTTTTTTCTTTTTTCTTTTTTTTTTTTTTTTTTGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCGCTGAGCTAAATCCCCAACCCT---------------------------------------------------------------------------------------------------------------------------40INTERGENIChomozygous60449313
2114415302114415303GGC9INTERGENIChomozygous59029990
2114417081114417082TC31INTERGENIChomozygous59029991
2114418641114418643AC--13INTERGENIChomozygous59029992
2114418824114418825CT28INTERGENIChomozygous59029993
2114419792114419793AT30INTERGENIChomozygous59029995
2114419934114419935T-14INTERGENIChomozygous59753144
2114419987114419988TC20INTERGENIChomozygous59029996
2114420874114420875GGA31INTERGENICpossibly homozygous59029997
2114420874114420875GGAA31INTERGENICheterozygous60574530
2114431384114431385CCAAA25INTERGENICpossibly homozygous59029998
2114431823114431837ACACACACACACAC--------------19INTERGENICpossibly homozygous60676673
2114433469114433479TGTGTGTGTG----------21INTERGENICheterozygous60676675
2114434188114434189AAAAAAAAAGC25INTERGENICpossibly homozygous59030002
2114434377114434378TC37INTERGENIChomozygous59030003
2114434378114434379GA37INTERGENIChomozygous59030004
2114439693114439694C-36INTERGENIChomozygous59030006
2114439707114439708GC38INTERGENIChomozygous59030007
2114441118114441119CCT15INTERGENIChomozygous59030008
2114441607114441608AAAT7INTERGENIChomozygous59030009
2114442505114442506A-8GENIChomozygous59030010
2114443851114443852GA21GENIChomozygous59030011
2114444380114444381GA23GENIChomozygous59030012
2114444449114444451AA--24GENICpossibly homozygous59030013
2114445060114445068AAAAAAAA--------14GENIChomozygous59030014
2114433473114433479TGTGTG------21INTERGENICpossibly homozygous61050202
2114434188114434189AAAAAAAAGC25INTERGENICheterozygous60494557