chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	160374737	160374738	A	T	20	GENIC	homozygous	114074135
5	160375033	160375034	G	A	39	GENIC	homozygous	114074136
5	160375595	160375596	T	C	25	GENIC	homozygous	114074137
5	160375688	160375689	C	T	31	GENIC	homozygous	114074138
5	160375704	160375705	G	A	29	GENIC	homozygous	114074139
5	160376076	160376077	T	C	47	GENIC	homozygous	114074141
5	160376188	160376189	C	T	20	GENIC	homozygous	114074142
5	160376548	160376549	T	C	23	GENIC	homozygous	114074143
5	160376681	160376682	A	C	25	GENIC	homozygous	114074144
5	160377062	160377063	C	T	37	GENIC	homozygous	114074145
5	160378129	160378130	A	T	31	GENIC	homozygous	114074146
5	160378197	160378198	C	G	31	GENIC	possibly homozygous	114074147
5	160378233	160378234	C	T	31	GENIC	homozygous	114074148
5	160378998	160378999	A	G	38	GENIC	homozygous	114074151
5	160379260	160379261	T	C	49	GENIC	homozygous	114074152
5	160379267	160379268	T	C	48	GENIC	homozygous	114074153
5	160379274	160379275	A	G	43	GENIC	homozygous	114074154
5	160379789	160379790	G	A	24	GENIC	homozygous	114074155
5	160380190	160380191	A	G	26	GENIC	possibly homozygous	114074156
5	160380505	160380506	T	C	9	GENIC	homozygous	114074157
5	160380722	160380723	G	C	30	GENIC	homozygous	114074158
5	160381401	160381402	G	A	44	GENIC	homozygous	114074159
5	160381437	160381438	T	C	41	GENIC	homozygous	114074160
5	160381576	160381577	G	A	23	GENIC	homozygous	114074161
5	160383001	160383002	C	T	38	GENIC	homozygous	114074162
5	160383368	160383369	G	A	43	GENIC	homozygous	114074163
5	160376856	160376857	G	C	25	GENIC	homozygous	114160888
5	160381784	160381785	C	A	19	GENIC	homozygous	114160890