chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11460032	11460033	A	C	27	GENIC	homozygous	115568362
7	11460123	11460124	G	A	19	GENIC	homozygous	115568363
7	11461159	11461160	T	C	32	GENIC	homozygous	115568364
7	11462270	11462271	A	G	44	GENIC	homozygous	115568365
7	11463424	11463425	C	T	31	GENIC	homozygous	115568367
7	11465224	11465225	G	A	29	GENIC	homozygous	115568368
7	11466052	11466053	T	C	25	GENIC	homozygous	115568369
7	11466155	11466156	C	A	33	GENIC	homozygous	115568370
7	11466174	11466175	A	C	33	GENIC	homozygous	115568372
7	11467567	11467568	T	C	35	GENIC	homozygous	115568373
7	11468451	11468452	A	T	37	GENIC	homozygous	115568374
7	11470069	11470070	A	G	30	GENIC	homozygous	115568375
7	11471868	11471869	T	C	39	GENIC	homozygous	115568376
7	11472135	11472136	C	T	38	GENIC	homozygous	115568377
7	11472325	11472326	G	A	37	GENIC	homozygous	115568378
7	11473542	11473543	T	C	25	GENIC	homozygous	118250958
7	11473543	11473544	C	A	25	GENIC	homozygous	118250961
7	11475386	11475387	A	G	32	GENIC	homozygous	115568379
7	11476130	11476131	A	G	33	GENIC	homozygous	115568380
7	11476471	11476472	C	T	41	GENIC	homozygous	115568381
7	11477120	11477121	T	G	19	GENIC	homozygous	115568383
7	11477160	11477161	T	C	17	GENIC	homozygous	115568384
7	11477392	11477393	T	C	28	GENIC	homozygous	115568385
7	11478272	11478273	C	T	16	GENIC	possibly homozygous	115568386