chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	11054499	11054500	T	C	26	GENIC	homozygous	115567900
7	11055171	11055172	G	A	19	GENIC	homozygous	115567901
7	11056124	11056125	C	A	15	GENIC	homozygous	115567902
7	11056966	11056967	A	G	25	GENIC	homozygous	115567903
7	11057452	11057453	A	G	18	GENIC	possibly homozygous	115567904
7	11058936	11058937	A	T	20	GENIC	homozygous	115567907
7	11059847	11059848	G	C	32	GENIC	homozygous	115567908
7	11060209	11060210	G	T	28	GENIC	homozygous	115567909
7	11060245	11060246	T	C	22	GENIC	homozygous	115567910
7	11060289	11060290	G	A	27	GENIC	homozygous	115567911
7	11060290	11060291	C	A	29	GENIC	homozygous	115567912
7	11060371	11060372	C	A	25	GENIC	homozygous	115567913
7	11061036	11061037	A	G	25	GENIC	homozygous	115567914
7	11061072	11061073	G	A	27	GENIC	homozygous	115567915
7	11061232	11061233	G	T	29	GENIC	homozygous	115567916
7	11061324	11061325	A	G	35	GENIC	homozygous	115567917
7	11069186	11069187	C	T	33	GENIC	homozygous	115567918
7	11072632	11072633	T	G	16	GENIC	homozygous	115567924
7	11074261	11074262	A	G	33	GENIC	homozygous	115567925
7	11074949	11074950	T	A	24	GENIC	homozygous	115567926
7	11075108	11075109	G	A	24	GENIC	homozygous	115567927