chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	46080183	46080183		TCAAGGTAG	18	GENIC	homozygous	140221179
18	46080313	46080314	T	C	14	GENIC	homozygous	140307147
18	46080831	46080832	A	G	16	GENIC	homozygous	140307148
18	46082660	46082661	C	A	22	GENIC	homozygous	140307149
18	46083957	46083958	A	T	13	GENIC	homozygous	140307150
18	46085365	46085367	AA		17	GENIC	homozygous	140221181
18	46085559	46085560	C	A	18	GENIC	homozygous	140307151
18	46088227	46088228	G	A	18	GENIC	homozygous	140307152
18	46088233	46088234	A	T	18	GENIC	homozygous	140307153
18	46088566	46088567	T	G	24	GENIC	homozygous	140307154
18	46089094	46089095	C	T	13	GENIC	homozygous	140307155
18	46089524	46089525	T	G	17	GENIC	homozygous	140307156
18	46090290	46090290		T	14	GENIC	homozygous	140221182
18	46090352	46090353	A	G	18	GENIC	homozygous	140307162
18	46089807	46089808	A	G	10	GENIC	homozygous	140307157
18	46090073	46090074	T	C	17	GENIC	homozygous	140307158
18	46090293	46090294	A	T	16	GENIC	homozygous	140307159
18	46090339	46090340	C	T	17	GENIC	homozygous	140307160
18	46090351	46090352	C	T	18	GENIC	homozygous	140307161
18	46091412	46091413	C	A	26	GENIC	homozygous	140307163
18	46092177	46092178	A	G	16	GENIC	homozygous	140307164
18	46092589	46092590	A	T	19	GENIC	homozygous	140307165
18	46092676	46092677	C	T	22	GENIC	homozygous	140307166
18	46093310	46093311	G		15	GENIC	homozygous	140221183
18	46093720	46093721	G	A	13	GENIC	homozygous	140307167
18	46094939	46094940	C	T	16	GENIC	homozygous	140307168
18	46095011	46095012	C	T	21	GENIC	homozygous	140307169
18	46095559	46095565	CCTCCT		6	GENIC	homozygous	140221184
18	46096892	46096892		T	10	GENIC	possibly homozygous	140221185
18	46098564	46098565	T		19	GENIC	homozygous	140221186
18	46098632	46098633	T	G	24	GENIC	homozygous	140307170