chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	174552617	174552618	A	G	60	GENIC	homozygous	136373306
2	174554627	174554628	A	G	38	GENIC	homozygous	136373307
2	174557433	174557434	A	T	23	GENIC	homozygous	136373308
2	174557465	174557466	A	G	33	GENIC	homozygous	154018975
2	174559652	174559653	C	G	38	GENIC	possibly homozygous	154018979
2	174559656	174559657	C	G	38	GENIC	possibly homozygous	154018981
2	174559660	174559661	C	G	38	GENIC	possibly homozygous	154018983
2	174559660	174559661	C		38	GENIC	heterozygous	403028009
2	174559635	174559636	A	G	38	GENIC	homozygous	136373309
2	174557465	174557466	A		33	GENIC	heterozygous	403028004
2	174559652	174559653	C		38	GENIC	heterozygous	403028005
2	174559656	174559657	C		38	GENIC	heterozygous	403028007
2	174557456	174557457	G	A	23	GENIC	homozygous	403707951
2	174557456	174557457	G		23	GENIC	heterozygous	403707952
2	174560693	174560694	T	C	37	GENIC	homozygous	136373310
2	174562661	174562662	G	A	40	GENIC	homozygous	136373311
2	174567329	174567330	C	T	52	GENIC	homozygous	136373312
2	174563605	174563607	CA		38	GENIC	homozygous	135961220
2	174559639	174559641	AG		38	GENIC	homozygous	135961219