chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208121551	208121552	G	A	13	GENIC	homozygous	59357206
2	208122406	208122407	T	-	11	GENIC	homozygous	59357208
2	208122548	208122549	T	C	13	GENIC	homozygous	59357209
2	208122633	208122634	C	CA	5	GENIC	homozygous	60301256
2	208122690	208122691	T	-	1	GENIC	homozygous	59932015
2	208122947	208122948	A	C	11	GENIC	homozygous	59932016
2	208123238	208123240	AC	--	29	GENIC	homozygous	59932017
2	208123969	208123970	C	G	28	GENIC	homozygous	59932018
2	208127243	208127244	T	TG	2	GENIC	heterozygous	59932020
2	208127350	208127351	G	GC	4	GENIC	homozygous	59357214
2	208129346	208129349	GGG	---	6	GENIC	heterozygous	59932022
2	208129347	208129349	GG	--	6	GENIC	heterozygous	60082126
2	208129521	208129522	A	ATGTGTG	5	GENIC	heterozygous	59357215
2	208129521	208129522	A	ATGTGTGTGTG	5	GENIC	heterozygous	59932024
2	208129521	208129522	A	ATGTGTGTG	5	GENIC	heterozygous	60825914
2	208129659	208129660	G	C	28	GENIC	homozygous	60301257
2	208131052	208131053	A	G	13	GENIC	homozygous	59932025
2	208131411	208131412	C	CACTA	15	GENIC	homozygous	59932026
2	208132171	208132172	C	-	1	GENIC	homozygous	60158822