chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	174552617	174552618	A	G	12	GENIC	homozygous	136373306
2	174554627	174554628	A	G	29	GENIC	homozygous	136373307
2	174557430	174557431	A	T	5	GENIC	homozygous	141422401
2	174557433	174557434	A	T	8	GENIC	homozygous	136373308
2	174557453	174557454	G	A	5	GENIC	homozygous	154018974
2	174557465	174557466	A	G	10	GENIC	homozygous	154018975
2	174559635	174559636	A	G	10	GENIC	homozygous	136373309
2	174559652	174559653	C	G	11	GENIC	homozygous	154018979
2	174559656	174559657	C	G	11	GENIC	homozygous	154018981
2	174559656	174559657	C		11	GENIC	heterozygous	403028007
2	174557453	174557454	G		5	GENIC	heterozygous	403028003
2	174557465	174557466	A		10	GENIC	heterozygous	403028004
2	174559652	174559653	C		11	GENIC	heterozygous	403028005
2	174559660	174559661	C	G	11	GENIC	homozygous	154018983
2	174559660	174559661	C		11	GENIC	heterozygous	403028009
2	174560693	174560694	T	C	17	GENIC	homozygous	136373310
2	174562661	174562662	G	A	21	GENIC	homozygous	136373311
2	174567329	174567330	C	T	16	GENIC	homozygous	136373312
2	174563605	174563607	CA		18	GENIC	homozygous	135961220
2	174561613	174561614	T		18	GENIC	possibly homozygous	141135572
2	174559639	174559641	AG		11	GENIC	homozygous	135961219