chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17616390 17616391 C T 28 GENIC homozygous 809188123 14 17616500 17616501 G A 31 GENIC homozygous 809188124 14 17616969 17616970 T A 44 GENIC homozygous 809188125 14 17617742 17617743 C A 46 GENIC homozygous 809188126 14 17619228 17619229 T A 45 GENIC homozygous 809188127 14 17619988 17619989 G A 45 GENIC possibly homozygous 809188128 14 17620908 17620909 G A 38 GENIC possibly homozygous 809188129 14 17621382 17621383 T C 40 GENIC homozygous 809188130 14 17621514 17621515 C T 51 GENIC homozygous 809188131 14 17622199 17622200 C T 67 GENIC possibly homozygous 809188132 14 17622565 17622566 T A 53 GENIC possibly homozygous 809188133 14 17625259 17625260 G A 46 GENIC homozygous 809188134 14 17625421 17625422 A C 45 GENIC homozygous 809188135 14 17625885 17625886 A G 53 GENIC possibly homozygous 809188136 14 17627520 17627521 C T 24 GENIC homozygous 809188137 14 17629159 17629160 G T 48 GENIC homozygous 809188138 14 17630313 17630314 G A 55 GENIC homozygous 809188139 14 17630413 17630414 C G 51 GENIC homozygous 809188140