chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1231972625231972626GC17GENIChomozygous61118503
1231973075231973076AAT1GENIChomozygous61118505
1231973346231973347CT4GENIChomozygous61118507
1231973350231973351AG4GENIChomozygous61118509
1231973987231973988GC17GENIChomozygous61118513
1231975675231975676CG14GENICpossibly homozygous61118522
1231975702231975703GGGTTTTT1GENIChomozygous62302722
1231975706231975707GT1GENIChomozygous62302723
1231976651231976788GCAAGTCCTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC-----------------------------------------------------------------------------------------------------------------------------------------7GENICheterozygous62103372
1231976966231976967CT21GENIChomozygous61118534
1231977373231977374AG11GENICheterozygous61118536
1231977950231977951G-3GENIChomozygous61118538
1231977951231977952CA3GENIChomozygous62302724
1231978301231978302TC16GENIChomozygous61118540
1231978325231978326TG22GENIChomozygous61118542
1231978440231978441AG13GENIChomozygous61118544
1231978482231978483CT29GENIChomozygous61118545
1231978781231978782TC15GENIChomozygous61118547
1231980472231980473TC15GENICpossibly homozygous61118549
1231980653231980654AG3GENIChomozygous61118551
1231981185231981186C-15GENICpossibly homozygous61118555
1231982215231982216GT19GENIChomozygous61118561
1231982349231982350AG21GENICpossibly homozygous61118563