chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1678374277837428CT9GENIChomozygous64901991
1678379227837923GA15GENIChomozygous64901992
1678392407839241GA19GENIChomozygous64901996
1678418987841899AG21GENIChomozygous64305465
1678428937842894AG11GENIChomozygous64692693
1678436647843665GA19GENIChomozygous64834651
1678437117843712TC20GENIChomozygous64305473
1678437847843785TC26GENIChomozygous64692695
1678446967844697CT11GENIChomozygous64901999
1678452757845276GC19GENIChomozygous64902000
1678464487846449GA6GENIChomozygous64902001
1678464537846454GA6GENIChomozygous64902002
1678483207848321TC16GENIChomozygous64305489
1678484387848439GA5GENIChomozygous64692703
1678492217849222GA18GENIChomozygous64692705
1678512547851255GT16GENICpossibly homozygous64692707
1678530727853073AG8GENIChomozygous64305503
1678530967853097CT14GENIChomozygous64692711
1678535557853556GA16GENIChomozygous64692713
1678536007853601CA14GENIChomozygous64692715
1678536907853691GA23GENIChomozygous64692717
1678544807854481GA12GENIChomozygous64692719
1678470957847096TG17GENIChomozygous65034689
1678545717854572CT9GENIChomozygous64692721
1678548267854827GA20GENIChomozygous64692723
1678563427856343GA3GENIChomozygous64305507
1678566277856628CT7GENIChomozygous64305509
1678568517856852CT12GENIChomozygous64902006
1678575997857600TC13GENIChomozygous64305513
1678592607859261CT9GENIChomozygous64902008