chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208141645	208141646	G	C	6	GENIC	homozygous	59357239
2	208141687	208141688	T	TC	24	GENIC	homozygous	59357240
2	208142167	208142168	G	C	22	GENIC	homozygous	59357241
2	208142234	208142235	G	C	19	GENIC	homozygous	59357242
2	208142239	208142240	G	T	18	GENIC	possibly homozygous	59771535
2	208142249	208142250	A	T	18	GENIC	possibly homozygous	59357243
2	208142251	208142252	G	C	17	GENIC	homozygous	59357244
2	208142255	208142256	A	C	19	GENIC	homozygous	59357245
2	208142260	208142261	G	C	23	GENIC	possibly homozygous	59357246
2	208142262	208142263	G	-	18	GENIC	homozygous	59357247
2	208142317	208142318	C	T	33	GENIC	homozygous	60158828
2	208143325	208143326	C	CT	18	GENIC	heterozygous	59932032
2	208143326	208143327	T	-	18	GENIC	heterozygous	59357248
2	208148430	208148431	C	T	35	GENIC	homozygous	60158829
2	208148902	208148903	G	-	12	GENIC	homozygous	59357251