chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7141163610141163611AG30GENIChomozygous54157861
7141164637141164638AG30GENIChomozygous54157862
7141164750141164751GA27GENICpossibly homozygous54157863
7141164823141164824AT20GENIChomozygous54157864
7141164959141164960TG21GENIChomozygous54157865
7141165014141165015GA19GENIChomozygous54157866
7141165023141165024TC20GENIChomozygous54157867
7141165110141165111GA24GENIChomozygous54157868
7141165742141165743AAACACACACAC4GENIChomozygous55768357
7141165795141165796AT13GENIChomozygous54157869
7141165859141165860GGCACACA17GENICpossibly homozygous55363388
7141166252141166253TC19GENIChomozygous54157870
7141166355141166356CT23GENIChomozygous54157871
7141166814141166815TA21GENIChomozygous54157872
7141167190141167191GA30GENIChomozygous54157873
7141167423141167424CT24GENIChomozygous54157874
7141167880141167881TC22GENIChomozygous54157875
7141165859141165860GGCACACACACA17GENICheterozygous55735471
7141168416141168417CCA11GENICheterozygous54265152
7141168416141168417CCAA11GENICheterozygous55032224
7141168660141168661AC17GENIChomozygous54157876