chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	231845942	231845943	A	C	34	GENIC	possibly homozygous	61118106
1	231847735	231847736	A	G	21	GENIC	homozygous	61118108
1	231849198	231849199	T	-	3	GENIC	homozygous	61118110
1	231849363	231849364	C	T	26	GENIC	possibly homozygous	61118112
1	231849975	231849976	A	G	39	GENIC	homozygous	61118113
1	231850297	231850298	T	A	30	GENIC	homozygous	61118115
1	231850316	231850317	T	C	21	GENIC	homozygous	61118116
1	231851532	231851533	A	T	42	GENIC	homozygous	61118119
1	231853003	231853004	T	TA	22	GENIC	homozygous	61118121
1	231853294	231853295	G	-	24	GENIC	homozygous	61118123
1	231853480	231853481	T	TA	16	GENIC	homozygous	61118125
1	231854937	231854938	G	A	29	GENIC	homozygous	61118127
1	231855970	231855971	A	G	20	GENIC	homozygous	61118129
1	231856251	231856252	T	TAC	9	GENIC	homozygous	61118131
1	231856338	231856339	C	CA	26	GENIC	homozygous	61118133
1	231857022	231857023	G	A	27	GENIC	homozygous	61118134
1	231857163	231857164	C	A	36	GENIC	possibly homozygous	61118136
1	231857946	231857947	C	CA	26	GENIC	homozygous	61118137
1	231857960	231857961	T	G	28	GENIC	possibly homozygous	61118139