chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	90212356	90212357	G	A	42	GENIC	possibly homozygous	68165197
10	90214912	90214913	T	A	33	GENIC	homozygous	68165200
10	90215154	90215155	G	A	41	GENIC	homozygous	68165203
10	90216961	90216962	T	C	59	GENIC	homozygous	68165206
10	90219690	90219691	G	T	58	GENIC	homozygous	68670018
10	90219906	90219907	C	A	22	GENIC	homozygous	68165210
10	90219935	90219936	C	G	13	GENIC	homozygous	68165213
10	90219940	90219941	T	G	12	GENIC	homozygous	68165216
10	90219945	90219946	C	A	10	GENIC	homozygous	68165219
10	90219951	90219952	C	A	11	GENIC	heterozygous	68165222
10	90224161	90224162	C	T	36	GENIC	homozygous	68165246
10	90224173	90224174	A	G	33	GENIC	homozygous	68165249
10	90226080	90226081	A	G	25	GENIC	homozygous	68165256
10	90229033	90229034	A	G	66	GENIC	homozygous	68165265
10	90230303	90230304	C	T	82	GENIC	possibly homozygous	68670020
10	90230370	90230371	G	A	56	GENIC	homozygous	68670022
10	90231521	90231522	G	C	50	GENIC	homozygous	68165271
10	90231805	90231806	G	C	48	GENIC	homozygous	68165274
10	90233044	90233045	T	C	73	GENIC	possibly homozygous	68165277
10	90233707	90233708	G	C	29	GENIC	heterozygous	68165283
10	90234636	90234637	A	G	70	GENIC	homozygous	68165286
10	90234685	90234686	A	G	74	GENIC	homozygous	68165289
10	90235845	90235846	G	T	66	GENIC	homozygous	68670024