chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11460032	11460033	A	C	37	GENIC	homozygous	115568362
7	11461159	11461160	T	C	29	GENIC	homozygous	115568364
7	11462270	11462271	A	G	50	GENIC	homozygous	115568365
7	11462675	11462676	A	C	18	GENIC	homozygous	115568366
7	11466052	11466053	T	C	30	GENIC	homozygous	115568369
7	11466155	11466156	C	A	42	GENIC	homozygous	115568370
7	11466160	11466161	C	T	41	GENIC	homozygous	116315971
7	11466161	11466162	A	G	43	GENIC	homozygous	115568371
7	11466174	11466175	A	C	50	GENIC	homozygous	115568372
7	11467567	11467568	T	C	50	GENIC	homozygous	115568373
7	11467980	11467981	G	A	34	GENIC	homozygous	116315973
7	11468451	11468452	A	T	26	GENIC	homozygous	115568374
7	11469809	11469810	A	T	32	GENIC	homozygous	116315975
7	11469920	11469921	G	A	37	GENIC	homozygous	116315977
7	11470069	11470070	A	G	29	GENIC	homozygous	115568375
7	11471868	11471869	T	C	43	GENIC	homozygous	115568376
7	11472135	11472136	C	T	41	GENIC	homozygous	115568377
7	11474741	11474742	G	T	38	GENIC	homozygous	116315979
7	11475386	11475387	A	G	46	GENIC	possibly homozygous	115568379
7	11475411	11475412	A	T	38	GENIC	homozygous	116273843
7	11476130	11476131	A	G	26	GENIC	homozygous	115568380
7	11476471	11476472	C	T	42	GENIC	homozygous	115568381
7	11476668	11476669	T	C	34	GENIC	homozygous	115568382
7	11477120	11477121	T	G	30	GENIC	homozygous	115568383
7	11477160	11477161	T	C	28	GENIC	homozygous	115568384
7	11477392	11477393	T	C	42	GENIC	homozygous	115568385
7	11478272	11478273	C	T	36	GENIC	homozygous	115568386