chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	145242009	145242010	T	C	26	GENIC	homozygous	136307134
2	145242512	145242513	T	A	24	GENIC	homozygous	136307135
2	145244025	145244026	T	A	10	GENIC	homozygous	403021519
2	145244025	145244026	T		10	GENIC	heterozygous	403021520
2	145244165	145244166	T	C	14	GENIC	homozygous	136307136
2	145244166	145244167	G	A	14	GENIC	homozygous	136307137
2	145244934	145244935	A	G	20	GENIC	homozygous	136307138
2	145245143	145245144	C	T	18	GENIC	homozygous	136307139
2	145245201	145245202	G	A	20	GENIC	homozygous	136307140
2	145245805	145245806	C	A	18	GENIC	homozygous	136307141
2	145245806	145245807	A	T	18	GENIC	homozygous	136307142
2	145245932	145245933	C	T	11	GENIC	homozygous	136307143
2	145245981	145245982	A	G	11	GENIC	homozygous	136307144
2	145246694	145246695	T	C	21	GENIC	homozygous	136307145
2	145246756	145246757	A	G	22	GENIC	homozygous	136307146
2	145247769	145247770	G	T	24	GENIC	homozygous	136307147
2	145247893	145247894	T	A	12	GENIC	homozygous	136307148
2	145244053	145244071	TGTGTGTGTGTGTGTGTA		9	GENIC	homozygous	141333197
2	145244725	145244726	G		13	GENIC	homozygous	135947587