chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	187143910	187143911	G	A	15	GENIC	homozygous	120377949
2	187143926	187143927	C	A	12	GENIC	possibly homozygous	120377950
2	187143936	187143937	G	A	11	GENIC	possibly homozygous	120377951
2	187143974	187143975	T	C	10	GENIC	possibly homozygous	120393690
2	187144404	187144405	A	C	24	GENIC	possibly homozygous	120377952
2	187145125	187145126	A	G	20	GENIC	possibly homozygous	120377953
2	187145795	187145796	G	A	23	GENIC	possibly homozygous	120377954
2	187145968	187145969	T	C	24	GENIC	possibly homozygous	120377955
2	187146154	187146155	C	T	29	GENIC	possibly homozygous	120377956
2	187146225	187146226	T	C	37	GENIC	possibly homozygous	120377957
2	187147311	187147312	A	C	24	GENIC	possibly homozygous	110166967
2	187147700	187147701	C	T	38	GENIC	homozygous	120377958
2	187148150	187148151	G	A	20	GENIC	possibly homozygous	110166968
2	187148907	187148908	A	G	27	GENIC	homozygous	110166969
2	187150174	187150175	T	C	21	GENIC	homozygous	110166971
2	187150330	187150331	T	C	16	GENIC	possibly homozygous	110166972
2	187151567	187151568	G	A	23	GENIC	homozygous	110166975
2	187152289	187152290	G	A	34	GENIC	possibly homozygous	120377959
2	187152461	187152462	A	G	22	GENIC	possibly homozygous	110166977
2	187153004	187153005	T	C	23	GENIC	homozygous	110166978
2	187153114	187153115	T	C	29	GENIC	homozygous	110166979
2	187154184	187154185	A	G	24	GENIC	homozygous	110166982
2	187156064	187156065	T	C	27	GENIC	homozygous	110166986