chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	40686193	40686194	G		45	GENIC	homozygous	129998290
20	40686213	40686213		A	45	GENIC	possibly homozygous	129998291
20	40687161	40687162	A		33	GENIC	homozygous	129998292
20	40687516	40687517	T		57	GENIC	possibly homozygous	129998293
20	40687614	40687615	T	C	49	GENIC	homozygous	130098045
20	40688040	40688041	A		43	GENIC	possibly homozygous	129998294
20	40688441	40688442	C	G	46	GENIC	homozygous	130098046
20	40688747	40688748	A	G	21	GENIC	homozygous	130098047
20	40688825	40688826	G	A	27	GENIC	homozygous	130098048
20	40688833	40688834	A	G	29	GENIC	homozygous	130098049
20	40688873	40688874	G	C	22	GENIC	homozygous	130098050
20	40689764	40689765	T	C	50	GENIC	possibly homozygous	130098051
20	40690231	40690231		G	30	GENIC	possibly homozygous	129998295
20	40690725	40690725		GCA	42	GENIC	homozygous	129998296
20	40690933	40690934	A		53	GENIC	homozygous	129998297
20	40689942	40689943	C	A	26	GENIC	heterozygous	403469759
20	40689942	40689943	C	G	26	GENIC	possibly homozygous	155149862