chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	93369376	93369377	A	T	6	GENIC	homozygous	117603462
9	93369713	93369714	T	C	13	GENIC	homozygous	117603464
9	93369716	93369717	G	C	15	GENIC	homozygous	117603466
9	93371356	93371357	T	C	24	GENIC	homozygous	117603468
9	93371613	93371614	A	G	8	GENIC	homozygous	117603470
9	93371920	93371921	A	G	15	GENIC	homozygous	117603472
9	93372053	93372054	A	G	19	GENIC	homozygous	117603474
9	93372180	93372181	A	G	10	GENIC	homozygous	117603476
9	93372638	93372639	C	T	9	GENIC	homozygous	117603478
9	93372869	93372870	T	G	14	GENIC	homozygous	117603480
9	93372988	93372989	G	A	9	GENIC	heterozygous	117603482
9	93372989	93372990	T	A	9	GENIC	homozygous	117603484
9	93373132	93373133	T	A	26	GENIC	homozygous	117603486
9	93373209	93373210	G	A	17	GENIC	homozygous	117603488
9	93373462	93373463	T	G	24	GENIC	homozygous	117603490
9	93374397	93374398	T	A	15	GENIC	heterozygous	117388945
9	93374736	93374737	C	T	21	GENIC	homozygous	117603492
9	93374813	93374814	C	A	7	GENIC	homozygous	117603494
9	93375321	93375322	A	G	20	GENIC	homozygous	117603496
9	93375617	93375618	T	C	24	GENIC	homozygous	117603498
9	93375734	93375735	T	C	14	GENIC	homozygous	117603500
9	93375762	93375763	G	C	21	GENIC	homozygous	117603502
9	93375943	93375944	A	G	10	GENIC	homozygous	117603504
9	93376285	93376286	T	C	19	GENIC	homozygous	117603506
9	93377603	93377604	C	T	16	GENIC	homozygous	117603508