chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	18354987	18354988	T	C	32	GENIC	homozygous	120186060
2	18355047	18355048	A	C	26	GENIC	homozygous	109620797
2	18355048	18355049	A	T	26	GENIC	homozygous	109620798
2	18355068	18355069	A	G	26	GENIC	homozygous	109620799
2	18355376	18355377	C	T	26	GENIC	homozygous	109620800
2	18356041	18356042	C	T	17	GENIC	homozygous	111319757
2	18356193	18356194	G	A	30	GENIC	homozygous	111319759
2	18356392	18356392		T	15	GENIC	homozygous	131800536
2	18356892	18356893	A	G	19	GENIC	homozygous	111319761
2	18356902	18356903	T		21	GENIC	homozygous	131800537
2	18357724	18357725	C	T	15	GENIC	homozygous	120430358
2	18357744	18357745	A	G	14	GENIC	homozygous	109620803
2	18358203	18358204	A	G	22	GENIC	homozygous	109620805
2	18362051	18362052	A	T	22	GENIC	homozygous	109620810
2	18368792	18368793	T	C	20	GENIC	homozygous	109620818
2	18371559	18371560	C	T	15	GENIC	homozygous	120430359
2	18392076	18392077	A	G	25	GENIC	homozygous	109620857
2	18390212	18390213	T	C	19	GENIC	homozygous	125786131
2	18395981	18395982	G	A	19	GENIC	homozygous	125786132
2	18400760	18400761	T	A	13	GENIC	homozygous	125786133
2	18415077	18415078	G	T	17	GENIC	homozygous	120121833
2	18415078	18415079	T	G	18	GENIC	homozygous	120121835
2	18415091	18415092	T		19	GENIC	homozygous	127596531
2	18415652	18415652		A	16	GENIC	homozygous	127596532
2	18416689	18416690	A	G	22	GENIC	homozygous	109620886