chr start stop reference nuc variant nuc depth genic status zygosity variant ID 8 58115537 58115538 T C 16 GENIC homozygous 634815236 8 58115551 58115555 ACTT ---- 16 GENIC homozygous 747675036 8 58115595 58115596 T TC 10 GENIC homozygous 747675037 8 58115651 58115652 A C 19 GENIC homozygous 634815237 8 58115867 58115868 T A 12 GENIC possibly homozygous 634815238 8 58116197 58116198 A C 24 GENIC homozygous 634815239 8 58116534 58116535 G T 41 GENIC homozygous 634815240 8 58117192 58117193 G A 30 GENIC possibly homozygous 634815241 8 58117647 58117648 A C 23 GENIC homozygous 634815242 8 58117683 58117684 G A 25 GENIC homozygous 634815243 8 58117711 58117712 A G 27 GENIC homozygous 634815244 8 58117726 58117727 A G 29 GENIC homozygous 634815245 8 58118150 58118151 T C 34 GENIC homozygous 634815246 8 58119235 58119236 A ATGTTGTTGT 18 GENIC homozygous 747675038 8 58119370 58119371 T C 27 GENIC homozygous 634815247 8 58119567 58119568 T C 35 GENIC homozygous 634815248 8 58119903 58119904 C T 29 GENIC homozygous 634815249 8 58120264 58120265 T TCTC 36 GENIC homozygous 747675040 8 58120675 58120676 C T 25 GENIC homozygous 634815250 8 58120715 58120716 G C 26 GENIC homozygous 634815251 8 58121010 58121011 A G 36 GENIC possibly homozygous 634815252 8 58121405 58121406 A G 39 GENIC homozygous 634815253