chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	117516826	117516827	C	G	32	GENIC	homozygous	115847407
7	117520169	117520170	A	G	38	GENIC	homozygous	115847419
7	117521513	117521514	G	C	47	GENIC	homozygous	115847421
7	117521820	117521821	G	A	35	GENIC	homozygous	115847423
7	117521872	117521873	G	A	34	GENIC	homozygous	115847425
7	117523204	117523205	C	T	24	GENIC	homozygous	115847427
7	117524352	117524353	G	A	41	GENIC	homozygous	115847429
7	117526576	117526577	C	T	59	GENIC	homozygous	115847433
7	117526587	117526588	G	A	54	GENIC	homozygous	115847435
7	117526635	117526636	C	T	49	GENIC	homozygous	115847437
7	117526958	117526959	T	C	48	GENIC	homozygous	115847439
7	117528304	117528305	G	A	39	GENIC	homozygous	115847441
7	117528960	117528961	C	T	38	GENIC	homozygous	115847443
7	117529078	117529079	T	G	61	GENIC	homozygous	115847445
7	117529191	117529192	T	C	44	GENIC	homozygous	115847447
7	117529808	117529809	G	A	43	GENIC	homozygous	115847449
7	117529849	117529850	G	T	61	GENIC	possibly homozygous	115847451
7	117533357	117533358	G	A	43	GENIC	homozygous	115847453
7	117534285	117534286	C	T	41	GENIC	homozygous	115847455
7	117537439	117537440	G	A	34	GENIC	homozygous	115847457