chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208122406	208122407	T	-	36	GENIC	homozygous	59357208
2	208122548	208122549	T	C	42	GENIC	homozygous	59357209
2	208122689	208122691	CT	--	18	GENIC	homozygous	59357210
2	208122690	208122691	T	-	19	GENIC	homozygous	59932015
2	208123237	208123238	A	AAC	29	GENIC	homozygous	60340571
2	208123969	208123970	C	G	59	GENIC	homozygous	59932018
2	208124736	208124737	A	C	34	GENIC	possibly homozygous	60340573
2	208126360	208126361	G	A	51	GENIC	homozygous	60340575
2	208127243	208127244	T	TG	9	GENIC	heterozygous	59932020
2	208127350	208127351	G	GC	24	GENIC	homozygous	59357214
2	208127360	208127361	C	T	30	GENIC	possibly homozygous	60340577
2	208129346	208129349	GGG	---	21	GENIC	heterozygous	59932022
2	208129521	208129522	A	ATGTGTGTGTG	5	GENIC	homozygous	59932024
2	208131411	208131412	C	CACTA	40	GENIC	homozygous	59932026
2	208132171	208132172	C	-	6	GENIC	heterozygous	60158822
2	208129347	208129349	GG	--	21	GENIC	possibly homozygous	60082126