chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	208120433	208120434	C	T	24	GENIC	homozygous	59932012
2	208120655	208120656	A	G	28	GENIC	homozygous	59932013
2	208121191	208121192	G	A	12	GENIC	homozygous	59932014
2	208122406	208122407	T	-	20	GENIC	homozygous	59357208
2	208122548	208122549	T	C	14	GENIC	homozygous	59357209
2	208122689	208122691	CT	--	6	GENIC	homozygous	59357210
2	208122690	208122691	T	-	6	GENIC	homozygous	59932015
2	208122947	208122948	A	C	13	GENIC	homozygous	59932016
2	208123238	208123240	AC	--	20	GENIC	homozygous	59932017
2	208123969	208123970	C	G	18	GENIC	homozygous	59932018
2	208126236	208126237	G	A	30	GENIC	homozygous	59932019
2	208127243	208127244	T	TG	2	GENIC	homozygous	59932020
2	208127350	208127351	G	GC	9	GENIC	homozygous	59357214
2	208129014	208129015	G	A	21	GENIC	homozygous	59932021
2	208129346	208129349	GGG	---	1	GENIC	homozygous	59932022
2	208129359	208129360	A	-	10	GENIC	heterozygous	59932023
2	208129521	208129522	A	ATGTGTGTGTG	5	GENIC	homozygous	59932024
2	208131052	208131053	A	G	13	GENIC	homozygous	59932025
2	208131411	208131412	C	CACTA	19	GENIC	homozygous	59932026
2	208132978	208132982	GTGT	----	6	GENIC	heterozygous	59932027