chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11679517	11679518	G	A	32	GENIC	homozygous	116274121
7	11696805	11696806	G	A	44	GENIC	homozygous	116274124
7	11696830	11696831	G	A	49	GENIC	homozygous	116274126
7	11700657	11700658	G	A	40	GENIC	heterozygous	116274127
7	11700661	11700662	G	A	42	GENIC	possibly homozygous	116274129
7	11702190	11702191	T	C	27	GENIC	homozygous	115568887
7	11702929	11702930	A	T	36	GENIC	homozygous	115568889
7	11706141	11706142	T	C	39	GENIC	homozygous	115568891
7	11706294	11706295	C	T	31	GENIC	homozygous	115568892
7	11706708	11706709	G	T	27	GENIC	homozygous	115568893
7	11707283	11707284	C	A	37	GENIC	homozygous	116274131
7	11707369	11707370	A	G	43	GENIC	homozygous	115568894
7	11708247	11708248	A	C	26	GENIC	homozygous	115568895
7	11708326	11708327	C	T	47	GENIC	homozygous	115568896
7	11708353	11708354	A	G	49	GENIC	homozygous	115568897
7	11708366	11708367	G	A	47	GENIC	homozygous	115568898
7	11709349	11709350	T	G	23	GENIC	homozygous	116316085
7	11709664	11709665	C	A	36	GENIC	homozygous	115568899
7	11709671	11709672	A	G	40	GENIC	homozygous	115568900