chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	41863267	41863268	A	G	41	GENIC	homozygous	74992151
1	41863271	41863272	T	C	40	GENIC	homozygous	74992152
1	41863824	41863825	A	G	36	GENIC	homozygous	74992153
1	41863907	41863908	G	C	22	GENIC	homozygous	74992154
1	41864570	41864571	A	G	26	GENIC	homozygous	74992155
1	41864642	41864643	A	G	24	GENIC	homozygous	74992156
1	41864679	41864680	T	G	20	GENIC	homozygous	74992157
1	41864930	41864931	A	T	41	GENIC	homozygous	74992158
1	41864946	41864947	G	A	33	GENIC	homozygous	74992159
1	41864992	41864993	C	T	30	GENIC	homozygous	74992160
1	41865590	41865591	T	A	27	GENIC	homozygous	74992161
1	41865740	41865741	C	T	26	GENIC	heterozygous	74992162
1	41865797	41865798	A	C	16	GENIC	heterozygous	74992163
1	41865937	41865938	A	G	15	GENIC	homozygous	74992164
1	41866900	41866901	A	T	29	GENIC	homozygous	74992165
1	41867361	41867362	G	C	35	GENIC	homozygous	74992166
1	41867660	41867661	C	G	19	GENIC	homozygous	74992167
1	41867775	41867776	A	G	30	GENIC	homozygous	74992168
1	41867917	41867918	T	G	16	GENIC	homozygous	74992169
1	41868107	41868108	T	C	17	GENIC	homozygous	74992170
1	41868423	41868424	C	A	28	GENIC	possibly homozygous	74992171
1	41868996	41868997	G	A	30	GENIC	homozygous	74992172
1	41869811	41869812	G	C	30	GENIC	homozygous	74992173