chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	48026041	48026042	G	A	39	GENIC	homozygous	108846111
1	48026157	48026158	T	C	38	GENIC	homozygous	108846112
1	48026322	48026323	A	G	34	GENIC	homozygous	108846113
1	48026450	48026451	A	G	43	GENIC	homozygous	108846114
1	48026476	48026477	T	C	46	GENIC	homozygous	108846115
1	48027049	48027050	A	G	24	GENIC	homozygous	108846117
1	48027647	48027648	C	T	9	GENIC	homozygous	108846118
1	48027681	48027682	A	G	12	GENIC	homozygous	108846119
1	48027726	48027727	C	G	18	GENIC	homozygous	108846120
1	48028101	48028102	C	T	13	GENIC	homozygous	108846121
1	48029712	48029713	T	C	20	GENIC	homozygous	108846122
1	48029994	48029995	G	T	27	GENIC	homozygous	108846123
1	48030099	48030100	A	G	35	GENIC	homozygous	108846124
1	48030135	48030136	G	C	36	GENIC	homozygous	108846125
1	48030738	48030739	A	T	30	GENIC	possibly homozygous	108846128
1	48030813	48030814	C	T	38	GENIC	homozygous	108846129
1	48031627	48031628	T	C	16	GENIC	homozygous	108846130
1	48032763	48032764	A	G	30	GENIC	homozygous	108846132
1	48033113	48033114	C	T	38	GENIC	homozygous	108846133