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	37	GENIC	homozygous	140114863
17	40133840	40133841	A	G	41	GENIC	homozygous	140114864
17	40133903	40134016	ATTGGACTACAGGGAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCACAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAAAAAGAACCAAAAAAA		33	GENIC	homozygous	140022386
17	40134775	40134776	A	C	37	GENIC	homozygous	140114865
17	40137821	40137822	A	G	33	GENIC	homozygous	140114870
17	40135831	40135832	A	G	50	GENIC	homozygous	140114866
17	40136302	40136303	G	A	38	GENIC	homozygous	140114867
17	40136472	40136473	A	G	30	GENIC	homozygous	140114868
17	40137247	40137248	T	C	44	GENIC	homozygous	140114869
17	40138435	40138436	C	T	20	GENIC	possibly homozygous	140114871
17	40139133	40139134	A	G	47	GENIC	homozygous	140114872
17	40139218	40139218		C	40	GENIC	homozygous	140022387
17	40140780	40140781	G	T	34	GENIC	homozygous	140114873
17	40142462	40142463	C	T	41	GENIC	homozygous	140114874
17	40142877	40142878	T	C	49	GENIC	homozygous	140114875
17	40145002	40145003	A	G	42	GENIC	homozygous	140114876
17	40145250	40145251	G	A	43	GENIC	homozygous	140114877
17	40145349	40145350	G	A	36	GENIC	homozygous	140114878
17	40148699	40148700	T	C	57	GENIC	homozygous	140114879
17	40150210	40150211	G	A	28	GENIC	homozygous	140114880
17	40151433	40151434	T	C	49	GENIC	homozygous	140114881
17	40154752	40154753	C	G	35	GENIC	homozygous	140114882
17	40155687	40155688	C	T	34	GENIC	homozygous	140114883
17	40156777	40156778	A	G	35	GENIC	homozygous	140114884
17	40157038	40157038		TCTGAAAATAAGCATTTT	15	GENIC	homozygous	140022388
17	40157151	40157151		T	33	GENIC	possibly homozygous	140022389
17	40158589	40158590	T	G	40	GENIC	homozygous	140114885
17	40139144	40139145	C	T	44	GENIC	homozygous	145031395