chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	40132773	40132774	A	C	37	GENIC	homozygous	140114862
17	40133388	40133389	G	A	35	GENIC	homozygous	140114863
17	40133840	40133841	A	G	31	GENIC	homozygous	140114864
17	40133903	40134016	ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA		26	GENIC	homozygous	140022386
17	40134775	40134776	A	C	38	GENIC	homozygous	140114865
17	40135085	40135086	C	T	32	GENIC	homozygous	145906562
17	40135601	40135602	T	C	31	GENIC	homozygous	145906563
17	40136302	40136303	G	A	33	GENIC	homozygous	140114867
17	40136472	40136473	A	G	38	GENIC	homozygous	140114868
17	40137247	40137248	T	C	38	GENIC	homozygous	140114869
17	40137821	40137822	A	G	40	GENIC	homozygous	140114870
17	40139133	40139134	A	G	44	GENIC	homozygous	140114872
17	40139218	40139218		C	28	GENIC	homozygous	140022387
17	40140780	40140781	G	T	18	GENIC	homozygous	140114873
17	40142462	40142463	C	T	43	GENIC	homozygous	140114874
17	40142877	40142878	T	C	36	GENIC	homozygous	140114875
17	40145002	40145003	A	G	46	GENIC	homozygous	140114876
17	40145250	40145251	G	A	44	GENIC	homozygous	140114877
17	40148699	40148700	T	C	34	GENIC	homozygous	140114879
17	40151433	40151434	T	C	45	GENIC	homozygous	140114881
17	40152812	40152813	G	A	36	GENIC	homozygous	145906564
17	40154752	40154753	C	G	34	GENIC	homozygous	140114882
17	40156777	40156778	A	G	39	GENIC	homozygous	140114884
17	40157151	40157151		T	44	GENIC	homozygous	140022389
17	40151213	40151213		T	43	GENIC	possibly homozygous	145890830