chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59585114	59585115	C	A	6	GENIC	homozygous	116608381
10	59586887	59586888	A	T	22	GENIC	homozygous	116608385
10	59588881	59588882	T	C	13	GENIC	homozygous	116608389
10	59588999	59589000	A	G	11	GENIC	homozygous	117079635
10	59589470	59589471	G	A	19	GENIC	homozygous	117079636
10	59589541	59589542	A	C	22	GENIC	homozygous	117079638
10	59590158	59590159	C	G	33	GENIC	homozygous	116608393
10	59592082	59592083	T	C	13	GENIC	homozygous	116608399
10	59592622	59592623	T	C	35	GENIC	homozygous	116608401
10	59594223	59594224	G	T	14	GENIC	homozygous	117079640
10	59594820	59594821	T	C	32	GENIC	homozygous	116608409
10	59596514	59596515	G	C	17	GENIC	homozygous	117104130
10	59596632	59596633	C	A	19	GENIC	homozygous	117079641
10	59597833	59597834	G	T	23	GENIC	possibly homozygous	116788644
10	59598388	59598389	A	G	27	GENIC	homozygous	116608411
10	59598544	59598545	C	T	29	GENIC	homozygous	117079643
10	59599693	59599694	A	G	30	GENIC	homozygous	116608413
10	59606503	59606504	C	T	15	GENIC	homozygous	117104132
10	59607026	59607027	T	C	25	GENIC	homozygous	116608415
10	59607426	59607427	C	G	17	GENIC	homozygous	117079645