chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	123599663	123599664	T	A	70	INTERGENIC	heterozygous	54090423
7	123599721	123599722	A	G	90	INTERGENIC	heterozygous	54090424
7	123599808	123599809	A	G	94	INTERGENIC	heterozygous	54090426
7	123599813	123599814	G	GT	89	INTERGENIC	heterozygous	54090427
7	123599827	123599828	G	A	100	INTERGENIC	heterozygous	54090428
7	123599844	123599845	G	A	100	INTERGENIC	heterozygous	54090430
7	123599847	123599848	T	C	101	INTERGENIC	heterozygous	54090431
7	123599976	123599977	C	G	102	INTERGENIC	heterozygous	54090432
7	123600041	123600042	C	A	98	INTERGENIC	heterozygous	54090433
7	123600985	123600986	G	A	50	INTERGENIC	homozygous	54090436
7	123601612	123601613	G	A	27	GENIC	heterozygous	54090437
7	123601633	123601634	C	G	26	GENIC	heterozygous	54090439
7	123601643	123601644	G	A	24	GENIC	heterozygous	54090440
7	123601654	123601655	C	T	24	GENIC	heterozygous	54090442
7	123601925	123601926	G	A	72	GENIC	heterozygous	54090443
7	123601970	123601971	C	T	83	GENIC	heterozygous	54090445
7	123602532	123602533	T	G	55	GENIC	homozygous	54090446
7	123602969	123602970	T	C	42	GENIC	possibly homozygous	54090448
7	123603020	123603021	G	T	52	GENIC	possibly homozygous	54090449
7	123603052	123603053	G	T	51	GENIC	homozygous	54090451
7	123603099	123603100	A	G	43	GENIC	homozygous	54090452
7	123603119	123603120	C	A	29	GENIC	possibly homozygous	54090454
7	123603124	123603125	C	A	27	GENIC	possibly homozygous	54090456
7	123603190	123603191	C	T	36	GENIC	possibly homozygous	54090457
7	123603198	123603199	T	C	40	GENIC	possibly homozygous	54090459
7	123603270	123603271	T	G	31	GENIC	homozygous	54090460
7	123603570	123603571	A	G	8	GENIC	homozygous	54090462
7	123603578	123603579	T	C	9	GENIC	homozygous	54090463
7	123604102	123604103	G	A	50	GENIC	heterozygous	54090465
7	123604465	123604466	G	GTC	21	GENIC	heterozygous	54090467
7	123604497	123604498	G	C	54	GENIC	homozygous	54090468
7	123606581	123606582	A	G	41	INTERGENIC	homozygous	54090471
7	123605258	123605259	T	G	33	GENIC	homozygous	54090470