chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47031007	47031008	T	A	22	GENIC	homozygous	116773096
10	47031265	47031266	T	C	11	GENIC	heterozygous	117078159
10	47032178	47032179	G	C	11	GENIC	homozygous	116878163
10	47032269	47032270	C	T	22	GENIC	homozygous	116878165
10	47034997	47034998	G	A	16	GENIC	homozygous	116878167
10	47037307	47037308	A	T	18	GENIC	homozygous	116878169
10	47038446	47038447	T	C	22	GENIC	homozygous	116587131
10	47040071	47040072	A	T	8	GENIC	homozygous	116587133
10	47040996	47040997	C	T	18	GENIC	homozygous	116878172
10	47046239	47046240	C	T	16	GENIC	homozygous	116878180
10	47050456	47050457	A	G	17	GENIC	homozygous	116587137
10	47051521	47051522	G	C	22	GENIC	homozygous	116587139
10	47053807	47053808	G	A	6	GENIC	homozygous	116587149
10	47054618	47054619	C	T	17	GENIC	homozygous	116878182
10	47054924	47054925	A	G	13	GENIC	homozygous	116773104
10	47055257	47055258	C	A	15	GENIC	homozygous	116587153
10	47055572	47055573	A	G	19	GENIC	homozygous	116587155
10	47056003	47056004	A	G	13	GENIC	homozygous	116587157
10	47056243	47056244	C	T	22	GENIC	homozygous	116878186
10	47056402	47056403	T	C	13	GENIC	homozygous	116878188
10	47056666	47056667	T	A	29	GENIC	homozygous	116878190
10	47057885	47057886	C	T	15	GENIC	homozygous	116878192
10	47057905	47057906	A	T	18	GENIC	homozygous	116587159
10	47058394	47058395	T	G	15	GENIC	homozygous	116878194
10	47059032	47059033	T	C	13	GENIC	homozygous	116878196