chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1231972625231972626GC17GENIChomozygous61118503
1231973075231973076AAT25GENICpossibly homozygous61118505
1231973987231973988GC35GENIChomozygous61118513
1231974136231974137CCCCT19GENIChomozygous62486170
1231975263231975264CG18GENIChomozygous61118520
1231976349231976350GGC20GENIChomozygous62486171
1231976457231976461AAAG----11GENIChomozygous61118532
1231976966231976967CT26GENIChomozygous61118534
1231977373231977374AG30GENIChomozygous61118536
1231977950231977951G-24GENIChomozygous61118538
1231977951231977952CA24GENIChomozygous62302724
1231978301231978302TC17GENIChomozygous61118540
1231978440231978441AG37GENIChomozygous61118544
1231980472231980473TC39GENIChomozygous61118549
1231980653231980654AG20GENIChomozygous61118551
1231980664231980665T-5GENIChomozygous61118553
1231981185231981186C-24GENIChomozygous61118555
1231982215231982216GT31GENIChomozygous61118561
1231982349231982350AG29GENIChomozygous61118563
1231974860231974863AAA---10GENIChomozygous62372854
1231980660231980661GA15GENIChomozygous62372856
1231975722231975723GGT24GENIChomozygous62522067
1231980662231980663GA6GENIChomozygous62522069
1231976651231976788GCAAGTCCTACTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTCCGGAGCTGGGGACCGAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCCCC-----------------------------------------------------------------------------------------------------------------------------------------32GENIChomozygous62103372
1231981245231981246CT21GENIChomozygous62103373