chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	95200545	95200546	C	T	24	GENIC	homozygous	116827403
10	95201121	95201122	A	G	18	GENIC	homozygous	116687112
10	95201651	95201651		ATT	25	GENIC	homozygous	131709482
10	95203145	95203145		G	21	GENIC	homozygous	131709485
10	95206271	95206271		CCC	27	GENIC	homozygous	132694345
10	95206981	95206982	A	G	17	GENIC	possibly homozygous	116827421
10	95208776	95208777	C		19	GENIC	homozygous	131709491
10	95209217	95209218	T	C	21	GENIC	homozygous	116687116
10	95209344	95209344		AATAA	27	GENIC	homozygous	128848247
10	95202498	95202499	C	T	17	GENIC	homozygous	116955838
10	95203500	95203501	C	T	20	GENIC	homozygous	116955840
10	95206292	95206293	C	T	24	GENIC	homozygous	116955842
10	95207437	95207438	G	A	5	GENIC	heterozygous	117134126
10	95207439	95207440	G	A	5	GENIC	heterozygous	117134127
10	95208491	95208492	A	G	18	GENIC	homozygous	117088903
10	95208494	95208495	A	C	18	GENIC	homozygous	117088905
10	95209934	95209951	GCCACTTGGTCTGAGCC		24	GENIC	homozygous	132694346
10	95210960	95210961	G	T	24	GENIC	homozygous	116687119
10	95211008	95211008		A	28	GENIC	homozygous	128848248
10	95211291	95211293	TA		22	GENIC	homozygous	128848249
10	95211450	95211450		ACATTA	30	GENIC	homozygous	128848250