chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230213893	230213894	G	A	18	GENIC	homozygous	74936644
2	230214243	230214244	G	A	13	GENIC	homozygous	74441118
2	230215222	230215223	A	G	10	GENIC	homozygous	74936645
2	230215570	230215571	G	A	28	GENIC	homozygous	74936646
2	230215663	230215664	G	T	19	GENIC	homozygous	74936647
2	230219448	230219449	A	G	27	GENIC	homozygous	74441132
2	230219893	230219894	A	C	3	GENIC	homozygous	74936648
2	230221686	230221687	T	C	22	GENIC	homozygous	74441138
2	230224555	230224556	G	A	5	GENIC	homozygous	74936649
2	230225600	230225601	A	G	19	GENIC	homozygous	74936650
2	230228839	230228840	A	T	21	GENIC	homozygous	74441154
2	230229437	230229438	G	A	14	GENIC	homozygous	74936651
2	230229607	230229608	G	A	13	GENIC	homozygous	74441156
2	230231352	230231353	C	A	11	GENIC	heterozygous	74441162
2	230231362	230231363	G	C	10	GENIC	heterozygous	74441164
2	230231409	230231410	C	T	6	GENIC	heterozygous	74441168
2	230231452	230231453	A	G	25	GENIC	heterozygous	74441170
2	230231459	230231460	T	A	55	GENIC	heterozygous	74441172
2	230231529	230231530	A	G	96	GENIC	heterozygous	74441176
2	230231574	230231575	G	T	38	GENIC	heterozygous	74441180
2	230231817	230231818	C	G	16	GENIC	heterozygous	74936652
2	230234367	230234368	A	G	20	GENIC	heterozygous	74441198
2	230234637	230234638	T	G	11	GENIC	heterozygous	74936657
2	230231246	230231247	C	T	18	GENIC	heterozygous	78717049