chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	45462541	45462542	T	C	8	GENIC	homozygous	115854085
11	45462746	45462747	T	G	19	GENIC	possibly homozygous	115854087
11	45462893	45462894	G	A	20	GENIC	homozygous	115854089
11	45462907	45462908	C	T	21	GENIC	homozygous	115854091
11	45462938	45462939	C	T	18	GENIC	possibly homozygous	115854093
11	45463025	45463026	T	A	18	GENIC	homozygous	115854095
11	45463220	45463221	T	C	28	GENIC	homozygous	115854097
11	45463466	45463467	A	T	29	GENIC	possibly homozygous	115963446
11	45463467	45463468	G	A	29	GENIC	possibly homozygous	115854099
11	45463787	45463788	T	C	29	GENIC	possibly homozygous	115854103
11	45464122	45464123	G	A	23	GENIC	homozygous	115854105
11	45464173	45464174	C	T	34	GENIC	possibly homozygous	115854107
11	45464913	45464914	C	T	33	GENIC	homozygous	115854109
11	45465100	45465101	G	A	43	GENIC	possibly homozygous	115854111
11	45465707	45465708	C	T	26	GENIC	possibly homozygous	115854113
11	45465964	45465965	G	A	17	GENIC	homozygous	115854115
11	45467126	45467127	A	C	30	GENIC	possibly homozygous	115854117
11	45467553	45467554	T	C	24	GENIC	homozygous	115854119
11	45467973	45467974	G	A	29	GENIC	homozygous	115854121
11	45468237	45468238	C	G	23	GENIC	possibly homozygous	115854123
11	45468259	45468260	A	G	16	GENIC	homozygous	115854125
11	45468356	45468357	T	C	20	GENIC	homozygous	115854127
11	45469118	45469119	T	C	17	GENIC	possibly homozygous	115854129
11	45469514	45469515	T	G	23	GENIC	homozygous	115854133
11	45469988	45469989	T	C	22	GENIC	homozygous	115854135
11	45470133	45470134	G	A	30	GENIC	possibly homozygous	115854137
11	45470382	45470383	C	T	39	GENIC	homozygous	115854139
11	45470443	45470444	G	A	22	GENIC	homozygous	115854141
11	45471077	45471078	T	C	28	GENIC	possibly homozygous	115854143
11	45471491	45471492	T	C	22	GENIC	homozygous	115854145
11	45471854	45471855	A	T	27	GENIC	homozygous	115854147
11	45471869	45471870	G	A	25	GENIC	homozygous	115854149
11	45472360	45472361	C	T	28	GENIC	possibly homozygous	115854151