chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2607460	2607461	T	C	15	GENIC	homozygous	115545462
7	2608570	2608571	A	C	15	GENIC	homozygous	115545466
7	2608926	2608926		A	16	GENIC	homozygous	128432304
7	2611456	2611457	C	G	19	GENIC	homozygous	115545468
7	2614873	2614874	C	G	8	GENIC	heterozygous	122715619
7	2614876	2614877	A	G	8	GENIC	heterozygous	122715620
7	2614877	2614878	T	C	8	GENIC	heterozygous	122715621
7	2614879	2614880	T	C	9	GENIC	heterozygous	122715622
7	2614883	2614884	G	A	10	GENIC	heterozygous	116311299
7	2610499	2610500	G	A	13	GENIC	homozygous	116311293
7	2614256	2614257	G	A	19	GENIC	homozygous	116311294
7	2614837	2614838	C	T	11	GENIC	heterozygous	116311296
7	2614859	2614860	A	G	7	GENIC	heterozygous	116311297
7	2612705	2612705		A	12	GENIC	homozygous	131006974
7	2614833	2614833		TT	12	GENIC	heterozygous	131006975
7	2614930	2614930		G	20	GENIC	homozygous	131006976
7	2614931	2614931		AAAAAG	20	GENIC	homozygous	131006977
7	2615282	2615282		A	8	GENIC	possibly homozygous	131006978
7	2615968	2615969	A	G	22	GENIC	homozygous	115545472
7	2618185	2618185		TG	8	GENIC	homozygous	131006979
7	2618792	2618793	T	C	10	GENIC	homozygous	115545474