chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	59585114	59585115	C	A	73	GENIC	homozygous	116608381
10	59586028	59586029	A	G	45	GENIC	homozygous	116608383
10	59586887	59586888	A	T	67	GENIC	homozygous	116608385
10	59588440	59588441	A	G	53	GENIC	homozygous	116608387
10	59588881	59588882	T	C	38	GENIC	homozygous	116608389
10	59589850	59589851	G	T	39	GENIC	homozygous	116608391
10	59590158	59590159	C	G	50	GENIC	homozygous	116608393
10	59591705	59591706	T	C	60	GENIC	homozygous	116608395
10	59591822	59591823	C	T	63	GENIC	homozygous	116608397
10	59592082	59592083	T	C	67	GENIC	homozygous	116608399
10	59592622	59592623	T	C	79	GENIC	homozygous	116608401
10	59592623	59592624	C	T	79	GENIC	homozygous	116608403
10	59592941	59592942	C	T	77	GENIC	homozygous	116608405
10	59593028	59593029	T	C	81	GENIC	homozygous	116608407
10	59594820	59594821	T	C	71	GENIC	homozygous	116608409
10	59596458	59596459	T	A	30	GENIC	homozygous	117060964
10	59598388	59598389	A	G	67	GENIC	homozygous	116608411
10	59599693	59599694	A	G	65	GENIC	homozygous	116608413
10	59607026	59607027	T	C	66	GENIC	homozygous	116608415
10	59596706	59596706		ACAA	66	GENIC	homozygous	128820865
10	59597398	59597399	T	G	52	GENIC	heterozygous	116890523