chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2518596	2518597	T	A	16	GENIC	possibly homozygous	115545328
7	2519342	2519343	A	G	60	GENIC	homozygous	115545330
7	2520459	2520460	G	T	35	GENIC	homozygous	115545332
7	2521706	2521707	G	A	30	GENIC	homozygous	115545334
7	2525558	2525559	A	T	26	GENIC	possibly homozygous	115545336
7	2526311	2526312	T	A	16	GENIC	homozygous	115545338
7	2527166	2527167	A	G	50	GENIC	homozygous	115545340
7	2527927	2527928	C	T	35	GENIC	homozygous	115545342
7	2528097	2528098	G	A	60	GENIC	homozygous	115545344
7	2528338	2528339	C	G	45	GENIC	heterozygous	115545346
7	2530748	2530749	A	C	43	GENIC	possibly homozygous	115545348
7	2531039	2531040	T	G	22	GENIC	possibly homozygous	115545350
7	2531347	2531348	A	G	48	GENIC	possibly homozygous	115545352
7	2532462	2532463	G	T	20	GENIC	homozygous	115545354
7	2532591	2532592	T	C	24	GENIC	homozygous	115545356
7	2532969	2532970	T	G	36	GENIC	possibly homozygous	115545358
7	2533729	2533730	C	A	37	GENIC	homozygous	115545360
7	2534981	2534982	C	T	31	GENIC	possibly homozygous	115545362
7	2537348	2537349	A	G	39	GENIC	homozygous	115545364
7	2540966	2540967	C	T	37	GENIC	possibly homozygous	115545366
7	2543058	2543059	T	C	56	GENIC	homozygous	115545368
7	2545101	2545102	T	C	59	GENIC	homozygous	115545370
7	2547417	2547418	A	C	36	GENIC	homozygous	115545372