chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	86375519	86375520	A	T	61	GENIC	homozygous	138842256
10	86375863	86375864	T	C	57	GENIC	homozygous	138842258
10	86375987	86375988	G	A	59	GENIC	homozygous	143463658
10	86376306	86376307	A	C	73	GENIC	homozygous	143463659
10	86376437	86376438	A	C	43	GENIC	homozygous	143463660
10	86377048	86377049	T	G	45	GENIC	homozygous	143463661
10	86377072	86377081	AAGTGTAGA		28	GENIC	possibly homozygous	144077615
10	86377532	86377533	G	A	48	GENIC	homozygous	138842260
10	86377607	86377608	G	A	51	GENIC	homozygous	143463662
10	86377736	86377737	A	G	52	GENIC	homozygous	143463663
10	86377785	86377786	G	T	51	GENIC	homozygous	143463664
10	86377889	86377890	C	T	57	GENIC	homozygous	143463665
10	86377925	86377926	G	A	54	GENIC	homozygous	143463666
10	86377981	86377982	A	G	61	GENIC	homozygous	143463667
10	86378627	86378628	C	T	57	GENIC	homozygous	143463668
10	86378731	86378732	C	G	40	GENIC	homozygous	138842264
10	86378775	86378776	G	A	45	GENIC	homozygous	143463669
10	86377158	86377159	C	A	43	GENIC	heterozygous	144873152
10	86377121	86377122	C	T	29	GENIC	heterozygous	154660060
10	86377176	86377177	T	C	47	GENIC	heterozygous	154660062
10	86377251	86377252	G	A	62	GENIC	heterozygous	154660063
10	86378279	86378279		T	57	GENIC	homozygous	138697007
10	86378154	86378154		AC	56	GENIC	homozygous	143435106
10	86379082	86379083	T		48	GENIC	homozygous	143435107
10	86377083	86377084	G		30	GENIC	possibly homozygous	144412421
10	86377086	86377088	GG		30	GENIC	heterozygous	144412422
10	86377092	86377095	GTC		27	GENIC	heterozygous	144412423
10	86377121	86377122	C		29	GENIC	heterozygous	403293769
10	86377176	86377177	T		47	GENIC	heterozygous	403293770
10	86377251	86377252	G		62	GENIC	heterozygous	403293771