chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	143841379	143841380	G	A	65	GENIC	homozygous	116100819
7	143841528	143841529	G	A	84	GENIC	homozygous	116100821
7	143843057	143843058	T	C	35	GENIC	homozygous	115944720
7	143844008	143844009	G	A	71	GENIC	homozygous	116100823
7	143844792	143844793	C	T	69	GENIC	homozygous	116100825
7	143846051	143846052	G	T	50	GENIC	homozygous	115944721
7	143848634	143848635	G	A	59	GENIC	homozygous	116100827
7	143842972	143842972		CTGAA	31	GENIC	homozygous	131026107
7	143851295	143851295		T	43	GENIC	possibly homozygous	130765679
7	143850474	143850486	GCGTTGGCGGGG		35	GENIC	homozygous	128531509
7	143855331	143855332	T	C	59	GENIC	homozygous	115944736
7	143857238	143857240	AC		20	GENIC	homozygous	131026108
7	143857250	143857258	ACACACAT		25	GENIC	homozygous	131026109
7	143857276	143857277	A	T	30	GENIC	homozygous	122879666
7	143857324	143857328	ACAT		28	GENIC	homozygous	131026111
7	143857333	143857343	CACACACACG		29	GENIC	possibly homozygous	131026112
7	143858097	143858098	G	T	42	GENIC	homozygous	116100833
7	143858472	143858473	C	T	66	GENIC	homozygous	116100835
7	143859650	143859651	C	T	62	GENIC	homozygous	116100837
7	143859828	143859829	C	G	37	GENIC	homozygous	115944738
7	143859876	143859877	G	A	42	GENIC	homozygous	116100839
7	143859977	143859978	T	C	49	GENIC	homozygous	116100841
7	143860101	143860101		T	56	GENIC	homozygous	131026113
7	143860111	143860123	CTTCTAAAAAGC		54	GENIC	homozygous	131026114
7	143860588	143860589	A	G	50	GENIC	homozygous	116100843
7	143861728	143861729	G		25	GENIC	possibly homozygous	131026115
7	143862081	143862082	C	T	53	GENIC	possibly homozygous	116100845