chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 69946465 69946466 C A 20 GENIC homozygous 531353862 14 69951302 69951303 G C 22 GENIC possibly homozygous 531353863 14 69951683 69951684 G GA 12 GENIC possibly homozygous 694651520 14 69951754 69951755 A AGG 12 GENIC homozygous 694651521 14 69952415 69952416 T G 14 GENIC possibly homozygous 531353864 14 69952520 69952521 G GAAA 12 GENIC possibly homozygous 694651522 14 69953576 69953577 G - 10 GENIC homozygous 694651523 14 69953607 69953608 G A 10 GENIC homozygous 531353865 14 69953611 69953612 G A 9 GENIC heterozygous 531353866 14 69953756 69953757 A G 13 GENIC homozygous 531353867 14 69954283 69954284 C T 11 GENIC homozygous 531353868 14 69955263 69955264 A AT 8 GENIC heterozygous 694651524 14 69955263 69955264 A ATT 8 GENIC possibly homozygous 694651525 14 69956318 69956319 A AGGT 17 GENIC homozygous 694651526 14 69956535 69956536 A ACG 6 GENIC homozygous 694651527 14 69956587 69956589 CG -- 2 GENIC homozygous 694651528 14 69956588 69956589 G - 2 GENIC homozygous 694651529 14 69956804 69956805 A C 5 GENIC homozygous 531353869 14 69956948 69956949 C T 3 GENIC homozygous 531353870 14 69956955 69956956 T A 3 GENIC homozygous 531353871 14 69958963 69958964 C T 12 GENIC homozygous 531353872 14 69961955 69961956 G A 14 GENIC homozygous 531353873 14 69962226 69962227 T C 11 GENIC possibly homozygous 531353874 14 69962858 69962859 C T 15 GENIC homozygous 531353875 14 69963494 69963495 A - 2 GENIC homozygous 694651530 14 69963501 69963502 G GT 2 GENIC homozygous 694651531 14 69966924 69966925 A - 5 GENIC homozygous 694651532 14 69967118 69967120 AA -- 8 GENIC heterozygous 694651533 14 69967119 69967120 A - 8 GENIC possibly homozygous 694651534 14 69969164 69969165 T TAAACAGTTAA 8 GENIC homozygous 694651535 14 69970522 69970523 G A 17 GENIC homozygous 531353876