chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	187144788	187144789	C	T	46	GENIC	homozygous	111343539
2	187146097	187146098	G	A	59	GENIC	homozygous	111343541
2	187146989	187146990	C		41	GENIC	homozygous	133081483
2	187148907	187148908	A	G	59	GENIC	homozygous	110166969
2	187147311	187147312	A	C	57	GENIC	homozygous	110166967
2	187148150	187148151	G	A	53	GENIC	homozygous	110166968
2	187149621	187149622	A	G	29	GENIC	homozygous	110166970
2	187150174	187150175	T	C	43	GENIC	homozygous	110166971
2	187150330	187150331	T	C	39	GENIC	homozygous	110166972
2	187151567	187151568	G	A	48	GENIC	homozygous	110166975
2	187151837	187151838	C	T	46	GENIC	homozygous	111343547
2	187152461	187152462	A	G	61	GENIC	homozygous	110166977
2	187153004	187153005	T	C	46	GENIC	homozygous	110166978
2	187153114	187153115	T	C	41	GENIC	homozygous	110166979
2	187153488	187153489	T	C	22	GENIC	homozygous	111343549
2	187153599	187153600	G	A	34	GENIC	homozygous	110166981
2	187154184	187154185	A	G	50	GENIC	homozygous	110166982
2	187154572	187154573	C	T	21	GENIC	homozygous	111343551
2	187155789	187155790	T	A	40	GENIC	homozygous	120213177
2	187156064	187156065	T	C	57	GENIC	homozygous	110166986
2	187155787	187155788	T		38	GENIC	homozygous	133081484