chr start stop reference nuc variant nuc depth genic status zygosity variant ID 9 93369376 93369377 A T 40 GENIC homozygous 929754593 9 93369713 93369714 T C 25 GENIC homozygous 929754594 9 93369716 93369717 G C 24 GENIC homozygous 929754595 9 93371356 93371357 T C 24 GENIC homozygous 929754596 9 93371613 93371614 A G 26 GENIC homozygous 929754597 9 93371920 93371921 A G 19 GENIC homozygous 929754598 9 93372053 93372054 A G 22 GENIC homozygous 929754599 9 93372180 93372181 A G 23 GENIC homozygous 929754600 9 93372638 93372639 C T 44 GENIC homozygous 929754601 9 93372869 93372870 T G 37 GENIC homozygous 929754602 9 93372988 93372989 G A 30 GENIC homozygous 929754603 9 93372989 93372990 T A 28 GENIC homozygous 929754604 9 93373132 93373133 T A 39 GENIC homozygous 929754605 9 93373209 93373210 G A 31 GENIC homozygous 929754606 9 93373462 93373463 T G 35 GENIC homozygous 929754607 9 93374736 93374737 C T 42 GENIC homozygous 929754608 9 93374813 93374814 C A 58 GENIC homozygous 929754609 9 93375321 93375322 A G 31 GENIC homozygous 929754610 9 93375617 93375618 T C 15 GENIC homozygous 929754611 9 93375734 93375735 T C 19 GENIC homozygous 929754612 9 93375762 93375763 G C 23 GENIC homozygous 929754613 9 93375943 93375944 A G 21 GENIC homozygous 929754614 9 93376285 93376286 T C 33 GENIC homozygous 929754615 9 93377603 93377604 C T 19 GENIC homozygous 929754616