chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 90733464 90733465 G GT 4 GENIC homozygous 769059684 9 90733496 90733497 G GT 13 GENIC homozygous 769059685 9 90734741 90734742 G A 27 GENIC possibly homozygous 671514375 9 90735731 90735732 A AGT 5 GENIC heterozygous 769059686 9 90736395 90736396 T G 16 GENIC possibly homozygous 671514376 9 90736878 90736879 T G 16 GENIC possibly homozygous 671514377 9 90736921 90736922 T G 11 GENIC homozygous 671514378 9 90736932 90736933 T G 4 GENIC homozygous 671514379 9 90736946 90736947 A G 2 GENIC homozygous 671514380 9 90736954 90736955 T G 3 GENIC homozygous 671514381 9 90736971 90736972 T A 7 GENIC homozygous 671514382 9 90739828 90739830 AA -- 7 GENIC homozygous 769059687 9 90741345 90741346 G A 12 GENIC heterozygous 671514383 9 90742424 90742426 TT -- 2 GENIC homozygous 769059688 9 90742610 90742611 C T 2 GENIC homozygous 671514384 9 90742611 90742612 C A 2 GENIC homozygous 671514385 9 90743837 90743838 C T 28 GENIC homozygous 671514386 9 90744298 90744299 T TC 4 GENIC homozygous 769059689 9 90745179 90745180 A T 6 GENIC heterozygous 671514387 9 90745586 90745587 T G 19 GENIC homozygous 671514388 9 90745645 90745646 A T 11 GENIC possibly homozygous 671514389 9 90745753 90745754 T A 13 GENIC heterozygous 671514390 9 90745955 90745956 A AC 10 GENIC homozygous 769059690 9 90745956 90745957 A T 11 GENIC homozygous 671514391 9 90746496 90746497 A C 18 GENIC homozygous 671514392 9 90746533 90746534 G - 17 GENIC homozygous 769059691 9 90748218 90748219 G C 3 GENIC homozygous 671514393 9 90748791 90748792 G GT 24 GENIC homozygous 769059692 9 90749695 90749696 G A 6 GENIC heterozygous 671514394