chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	159996063	159996064	T	C	26	GENIC	homozygous	111791119
3	159996198	159996199	A	G	27	GENIC	homozygous	111791121
3	159996640	159996641	C	T	6	GENIC	homozygous	111791125
3	159996681	159996682	G	A	25	GENIC	homozygous	111791127
3	159998011	159998012	A	G	15	GENIC	homozygous	111791129
3	159998032	159998033	G	T	12	GENIC	homozygous	125840814
3	159998102	159998103	A	G	9	GENIC	homozygous	111791131
3	159998898	159998899	C	G	11	GENIC	heterozygous	125840815
3	160000272	160000273	G	A	16	GENIC	homozygous	111791133
3	160005018	160005019	C	T	14	GENIC	homozygous	111791135
3	160008150	160008151	C	G	34	GENIC	homozygous	111791137
3	160009225	160009226	C	T	30	GENIC	homozygous	111791138
3	160010164	160010165	A	G	14	GENIC	homozygous	111791140
3	160010762	160010763	G	C	32	GENIC	homozygous	111791142
3	160011322	160011323	C	A	23	GENIC	homozygous	111791144
3	160011765	160011766	A	G	24	GENIC	homozygous	111791146
3	160013805	160013806	A	G	29	GENIC	homozygous	111791148
3	160014125	160014126	A	T	21	GENIC	homozygous	111791150
3	160014630	160014631	G	A	19	GENIC	homozygous	111791152