chr start stop reference nuc variant nuc depth genic status zygosity variant ID 5 159590044 159590045 C T 12 GENIC homozygous 961070913 5 159590355 159590356 A C 39 GENIC homozygous 961070914 5 159590356 159590357 G C 39 GENIC homozygous 961070915 5 159590377 159590378 G A 34 GENIC homozygous 961070916 5 159590516 159590517 A G 30 GENIC homozygous 961070917 5 159590543 159590544 T C 23 GENIC homozygous 961070918 5 159590567 159590568 T C 23 GENIC homozygous 961070919 5 159590810 159590811 G A 30 GENIC homozygous 961070920 5 159591041 159591042 C T 22 GENIC homozygous 961070921 5 159591165 159591166 A G 28 GENIC homozygous 961070922 5 159591294 159591295 G A 28 GENIC possibly homozygous 961070923 5 159591492 159591493 C T 36 GENIC homozygous 961070924 5 159591711 159591712 G A 22 GENIC homozygous 961070925 5 159591959 159591960 C T 25 GENIC homozygous 961070926 5 159592241 159592242 A G 23 GENIC homozygous 961070927 5 159592551 159592552 G A 35 GENIC homozygous 961070928 5 159592593 159592594 G A 34 GENIC homozygous 961070929 5 159592713 159592714 C T 33 GENIC homozygous 961070930 5 159593011 159593012 T A 23 GENIC homozygous 961070931 5 159593229 159593230 A G 32 GENIC homozygous 961070932 5 159593316 159593317 A C 26 GENIC homozygous 961070933 5 159594481 159594482 G A 35 GENIC homozygous 961070934 5 159595521 159595522 G A 22 GENIC homozygous 961070935 5 159598268 159598269 G A 32 GENIC homozygous 961070936 5 159599504 159599505 T C 19 GENIC homozygous 961070937 5 159600471 159600472 T C 22 GENIC homozygous 961070938 5 159601143 159601144 C T 32 GENIC homozygous 961070939 5 159601217 159601218 A G 33 GENIC homozygous 961070940 5 159601274 159601275 A G 29 GENIC homozygous 961070941 5 159602018 159602019 C T 11 GENIC homozygous 961070942