chr start stop reference nuc variant nuc depth genic status zygosity variant ID 14 17616390 17616391 C T 19 GENIC homozygous 967845565 14 17616500 17616501 G A 19 GENIC homozygous 967845566 14 17616969 17616970 T A 29 GENIC homozygous 967845567 14 17617742 17617743 C A 22 GENIC homozygous 967845568 14 17619228 17619229 T A 25 GENIC homozygous 967845569 14 17620908 17620909 G A 32 GENIC homozygous 967845570 14 17621382 17621383 T C 37 GENIC homozygous 967845571 14 17621514 17621515 C T 31 GENIC homozygous 967845572 14 17622199 17622200 C T 22 GENIC homozygous 967845573 14 17622565 17622566 T A 24 GENIC homozygous 967845574 14 17625259 17625260 G A 26 GENIC homozygous 967845575 14 17625421 17625422 A C 17 GENIC homozygous 967845576 14 17625885 17625886 A G 19 GENIC homozygous 967845577 14 17627520 17627521 C T 18 GENIC homozygous 967845578 14 17629159 17629160 G T 16 GENIC homozygous 967845579 14 17630313 17630314 G A 26 GENIC possibly homozygous 967845580 14 17630413 17630414 C G 19 GENIC possibly homozygous 967845581