chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
796757869675866ACAGACACACACACACTCACAGACACACAGATACACACACACACTCACAGAAACACAGATACACACACAGACACTCACAT19GENIChomozygous147550064
796760909676091AT13GENIChomozygous147551530
796761079676108GC14GENIChomozygous147551531
796761179676151CACACAGACACACAGATACAGACGCACACACACT13GENIChomozygous147550065
796762909676291TA14GENICpossibly homozygous147551532
796763169676317GA17GENICpossibly homozygous147551536
796762949676295AT15GENICpossibly homozygous147551533
796763019676302CA16GENICpossibly homozygous147551534
796763139676314GC18GENICpossibly homozygous147551535
796763219676322CG18GENICpossibly homozygous147551537
796765589676558ACAGACACACACACACAGACACACACAT17GENICheterozygous147550066
796766719676679CACAGACA29GENIChomozygous147550067
796811509681151CA61GENICpossibly homozygous147551538
796841409684148GACTCCCA41GENIChomozygous147550068
796845899684592CAT57GENIChomozygous147550069
796900069690007AG50GENIChomozygous138000420
796902629690263TC62GENIChomozygous138000422