chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263782121	263782122	C	T	34	GENIC	homozygous	108634095
1	263782141	263782142	A	G	32	GENIC	homozygous	108634097
1	263782637	263782638	G	C	35	GENIC	homozygous	108634099
1	263782745	263782746	A	G	47	GENIC	homozygous	108634101
1	263785197	263785198	C	T	25	GENIC	homozygous	108634103
1	263785842	263785843	T	C	33	GENIC	homozygous	108634104
1	263786735	263786736	G	A	43	GENIC	homozygous	108634106
1	263787737	263787738	T	C	35	GENIC	homozygous	108634108
1	263788357	263788358	T	C	19	GENIC	homozygous	108634110
1	263788823	263788824	A	G	27	GENIC	homozygous	108634112
1	263789047	263789048	C	T	34	GENIC	homozygous	108634114
1	263790673	263790674	A	G	31	GENIC	homozygous	108634118
1	263792077	263792078	G	T	26	GENIC	homozygous	108634120
1	263792649	263792650	A	G	30	GENIC	homozygous	108634124
1	263794569	263794570	G	A	27	GENIC	homozygous	108634128
1	263797888	263797889	C	A	42	GENIC	homozygous	108634135
1	263799307	263799308	G	A	29	GENIC	homozygous	108634137
1	263799381	263799382	C	T	40	GENIC	homozygous	108634139
1	263800824	263800825	T	C	43	GENIC	homozygous	108634141
1	263801337	263801338	C	T	35	GENIC	homozygous	108634143
1	263802103	263802104	C	T	24	GENIC	homozygous	108634147
1	263802794	263802795	A	C	33	GENIC	homozygous	108634149