chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	174877357	174877358	A	G	46	GENIC	homozygous	136373626
2	174878178	174878179	C	T	55	GENIC	homozygous	142965057
2	174878365	174878366	C	T	50	GENIC	homozygous	142965058
2	174878989	174878990	C	G	46	GENIC	homozygous	136373629
2	174880129	174880130	A	C	47	GENIC	homozygous	142965059
2	174880286	174880393	CAAAAAAATTATTATTGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAAGAAC		33	GENIC	homozygous	135961327
2	174881053	174881054	A	G	50	GENIC	homozygous	142965060
2	174881785	174881786	G	T	46	GENIC	homozygous	142965061
2	174881964	174881965	C	T	38	GENIC	homozygous	142965062
2	174882260	174882260		T	42	GENIC	possibly homozygous	135961328
2	174883953	174883954	T	C	37	GENIC	homozygous	136373635
2	174884616	174884617	A	T	49	GENIC	homozygous	142965063
2	174884829	174884830	T	C	62	GENIC	homozygous	142965064
2	174885430	174885431	T	C	50	GENIC	homozygous	136373636
2	174885883	174885884	C	T	52	GENIC	homozygous	136373637
2	174886089	174886090	C	T	71	GENIC	homozygous	136373638
2	174886229	174886230	A	G	52	GENIC	homozygous	136373639
2	174882047	174882056	TCTTTTTTC		32	GENIC	homozygous	142901034