chr start stop reference nuc variant nuc depth genic status zygosity variant ID 10 95363392 95363393 A G 23 GENIC homozygous 68186761 10 95363937 95363938 G A 11 GENIC homozygous 68186764 10 95364054 95364055 G A 25 GENIC homozygous 68186768 10 95364308 95364309 G A 15 GENIC homozygous 68186773 10 95364837 95364838 T C 16 GENIC homozygous 68186781 10 95365164 95365165 C T 20 GENIC homozygous 68186785 10 95365201 95365202 C T 22 GENIC homozygous 68186789 10 95366431 95366432 T G 18 GENIC homozygous 68186794 10 95366525 95366526 G A 23 GENIC homozygous 68186798 10 95369216 95369216 GTAA 9 GENIC homozygous 69644390 10 95371916 95371917 G A 8 GENIC homozygous 68186810 10 95371922 95371923 T A 9 GENIC homozygous 68186815 10 95373259 95373260 G A 17 GENIC homozygous 68186819 10 95373457 95373458 T C 18 GENIC homozygous 68186823 10 95374120 95374121 A G 14 GENIC homozygous 68186827 10 95374494 95374495 T C 25 GENIC homozygous 68186831 10 95375086 95375087 A 27 GENIC heterozygous 69280421 10 95376018 95376019 G A 17 GENIC homozygous 68186834 10 95378459 95378460 C A 19 GENIC homozygous 68186838 10 95378520 95378521 C T 16 GENIC homozygous 68186842 10 95378570 95378571 T C 19 GENIC homozygous 68186846 10 95378701 95378702 C T 15 GENIC homozygous 68186850 10 95378830 95378831 T C 21 GENIC homozygous 68186854 10 95378958 95378959 C T 20 GENIC homozygous 68186857 10 95379887 95379888 G A 17 GENIC homozygous 68186861 10 95380155 95380156 C T 4 GENIC homozygous 68186865 10 95380878 95380879 G A 6 GENIC homozygous 68186869 10 95381019 95381020 G A 14 GENIC homozygous 68186873