chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	2965705	2965706	G	A	10	GENIC	homozygous	53767285
7	2966496	2966497	A	T	16	GENIC	possibly homozygous	53767287
7	2967195	2967196	G	-	5	GENIC	homozygous	53767300
7	2967197	2967198	G	A	5	GENIC	homozygous	54883758
7	2968325	2968326	A	-	5	GENIC	heterozygous	53767302
7	2968405	2968406	T	C	6	GENIC	homozygous	53767304
7	2969603	2969604	G	A	13	GENIC	possibly homozygous	54706569
7	2970687	2970688	G	A	18	GENIC	homozygous	53767306
7	2970896	2970897	C	G	15	GENIC	possibly homozygous	53767308
7	2970967	2970968	C	T	7	GENIC	possibly homozygous	53767310
7	2971289	2971290	A	G	6	GENIC	heterozygous	53767312
7	2973686	2973687	C	CTCTGG	1	GENIC	homozygous	53767314
7	2974062	2974063	G	A	8	GENIC	homozygous	53767320
7	2974493	2974495	TG	--	20	GENIC	homozygous	54706571
7	2974892	2974893	A	G	16	GENIC	possibly homozygous	53767324
7	2975215	2975216	C	G	10	GENIC	possibly homozygous	53767328
7	2975881	2975882	C	G	6	GENIC	heterozygous	53767337
7	2976637	2976638	T	C	3	GENIC	homozygous	53767343
7	2976733	2976734	G	A	9	GENIC	homozygous	54706575
7	2977642	2977643	C	T	5	GENIC	heterozygous	54706577
7	2977789	2977790	G	A	11	GENIC	homozygous	53767350
7	2978076	2978077	G	C	10	GENIC	heterozygous	53767352
7	2978408	2978409	T	G	13	GENIC	possibly homozygous	54706579
7	2979121	2979122	C	T	10	GENIC	possibly homozygous	54706581
7	2982596	2982597	C	-	2	GENIC	homozygous	54165776
7	2983632	2983633	T	A	5	GENIC	homozygous	53767369
7	2984091	2984092	A	G	3	GENIC	homozygous	53767373
7	2984821	2984822	A	T	2	GENIC	heterozygous	53767380
7	2983593	2983594	A	AT	2	GENIC	homozygous	55547951
7	2972109	2972110	G	T	6	GENIC	heterozygous	55547947