chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	47031007	47031008	T	A	35	GENIC	homozygous	116773096
10	47032269	47032270	C	T	32	GENIC	homozygous	116878165
10	47034997	47034998	G	A	33	GENIC	homozygous	116878167
10	47037307	47037308	A	T	40	GENIC	homozygous	116878169
10	47038446	47038447	T	C	42	GENIC	homozygous	116587131
10	47040071	47040072	A	T	26	GENIC	homozygous	116587133
10	47040996	47040997	C	T	28	GENIC	homozygous	116878172
10	47045318	47045319	C	A	31	GENIC	homozygous	116587135
10	47050456	47050457	A	G	34	GENIC	homozygous	116587137
10	47051521	47051522	G	C	43	GENIC	homozygous	116587139
10	47052653	47052654	T	C	3	GENIC	homozygous	116587143
10	47053807	47053808	G	A	49	GENIC	homozygous	116587149
10	47054717	47054718	T	C	22	GENIC	possibly homozygous	117993596
10	47046239	47046240	C	T	58	GENIC	homozygous	116878180
10	47054618	47054619	C	T	46	GENIC	homozygous	116878182
10	47054797	47054798	G	A	21	GENIC	homozygous	116878184
10	47054924	47054925	A	G	47	GENIC	possibly homozygous	116773104
10	47055257	47055258	C	A	40	GENIC	homozygous	116587153
10	47056243	47056244	C	T	29	GENIC	homozygous	116878186
10	47056402	47056403	T	C	28	GENIC	homozygous	116878188
10	47056666	47056667	T	A	52	GENIC	homozygous	116878190
10	47056814	47056815	C	G	32	GENIC	heterozygous	117218297
10	47057885	47057886	C	T	49	GENIC	possibly homozygous	116878192
10	47057905	47057906	A	T	48	GENIC	possibly homozygous	116587159
10	47055572	47055573	A	G	45	GENIC	homozygous	116587155
10	47056003	47056004	A	G	34	GENIC	homozygous	116587157
10	47058394	47058395	T	G	49	GENIC	possibly homozygous	116878194
10	47059032	47059033	T	C	22	GENIC	homozygous	116878196
10	47058249	47058250	C	T	43	GENIC	homozygous	117008782
10	47058102	47058103	C	T	29	GENIC	heterozygous	117103799