chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	170621711	170621712	G	GA	31	GENIC	homozygous	61909297
1	170622756	170622757	T	C	37	GENIC	homozygous	60941111
1	170623122	170623123	C	A	21	GENIC	homozygous	60941112
1	170623281	170623282	T	C	21	GENIC	homozygous	61909298
1	170623994	170623995	G	C	39	GENIC	homozygous	61909299
1	170624336	170624337	T	TCACA	4	GENIC	homozygous	60941114
1	170624733	170624734	C	T	46	GENIC	homozygous	61909300
1	170625101	170625102	G	A	43	GENIC	homozygous	61909301
1	170625345	170625346	G	A	32	GENIC	homozygous	61909302
1	170626576	170626580	TAAA	----	19	GENIC	homozygous	61909303
1	170628280	170628281	G	A	36	GENIC	homozygous	61909304
1	170628709	170628710	A	G	41	GENIC	homozygous	60941115
1	170629076	170629077	A	-	1	GENIC	homozygous	61909305
1	170629637	170629638	G	A	39	GENIC	homozygous	60941117
1	170631272	170631273	G	A	36	GENIC	homozygous	61909306
1	170631445	170631446	T	C	42	GENIC	possibly homozygous	60941118
1	170631480	170631482	AC	--	13	GENIC	heterozygous	60941119
1	170631481	170631482	C	-	32	GENIC	homozygous	60941120
1	170632202	170632203	T	C	29	GENIC	homozygous	60941121
1	170632326	170632327	C	T	29	GENIC	homozygous	61909307
1	170632351	170632352	G	A	30	GENIC	homozygous	61909308