chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11265293	11265294	G	GTGGA	1	GENIC	homozygous	54181353
7	11266608	11266609	C	T	7	GENIC	homozygous	55549901
7	11266929	11266930	G	GCATGC	2	GENIC	homozygous	53787934
7	11267215	11267216	C	T	7	GENIC	homozygous	55549905
7	11267552	11267553	T	C	7	GENIC	homozygous	53787940
7	11268082	11268083	A	C	10	GENIC	possibly homozygous	53787942
7	11268463	11268464	G	C	11	GENIC	homozygous	53787943
7	11268583	11268584	T	C	15	GENIC	homozygous	53787945
7	11268613	11268614	T	G	16	GENIC	homozygous	53787947
7	11269390	11269391	A	C	4	GENIC	homozygous	53787952
7	11272117	11272118	A	G	8	GENIC	homozygous	53787955
7	11270479	11270480	G	A	9	GENIC	homozygous	55549908
7	11271249	11271250	C	T	11	GENIC	homozygous	53787953
7	11271390	11271391	C	T	7	GENIC	homozygous	55549911
7	11276633	11276634	G	A	2	GENIC	heterozygous	53787967
7	11277099	11277100	T	G	9	GENIC	possibly homozygous	53787970
7	11279590	11279591	T	C	4	GENIC	homozygous	53787988
7	11279645	11279646	T	G	8	GENIC	homozygous	53787990
7	11286472	11286473	G	-	5	GENIC	homozygous	53787999
7	11286495	11286496	G	A	9	GENIC	heterozygous	53788001
7	11286640	11286641	A	-	6	GENIC	heterozygous	53788004