chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	66714252	66714253	G	A	49	GENIC	homozygous	116047956
11	66716479	66716480	T	C	61	GENIC	homozygous	115888070
11	66716684	66716685	G	A	57	GENIC	homozygous	115888072
11	66717308	66717309	T	A	55	GENIC	homozygous	115888074
11	66717553	66717554	C	A	51	GENIC	homozygous	115888076
11	66717603	66717604	G	C	48	GENIC	homozygous	115888078
11	66717713	66717714	G	A	45	GENIC	homozygous	116047958
11	66718943	66718944	A	G	55	GENIC	possibly homozygous	115888080
11	66720984	66720985	T	A	51	GENIC	possibly homozygous	115888082
11	66722324	66722325	C	T	57	GENIC	homozygous	116047960
11	66717511	66717512	C	G	40	GENIC	homozygous	116266072
11	66723509	66723510	T	C	53	GENIC	homozygous	115888092
11	66724112	66724113	A	C	50	GENIC	homozygous	115888096
11	66724228	66724229	T	C	50	GENIC	homozygous	115888098
11	66725434	66725435	T	C	54	GENIC	homozygous	115888106
11	66726361	66726362	T	C	77	GENIC	homozygous	115888110
11	66726754	66726755	G	C	54	GENIC	homozygous	115888114
11	66727346	66727347	A	G	63	GENIC	homozygous	115888116
11	66729088	66729089	A	T	49	GENIC	homozygous	116047962
11	66729590	66729591	A	T	72	GENIC	homozygous	116047964
11	66729697	66729698	T	C	61	GENIC	homozygous	116047966
11	66728869	66728870	A	C	31	GENIC	possibly homozygous	115977397
11	66717452	66717460	TCTCTCTT		16	GENIC	possibly homozygous	132155982
11	66717462	66717486	TCTCTCTTTCTGTGTGTGTGTGTG		17	GENIC	heterozygous	128918713
11	66728815	66728815		G	47	GENIC	homozygous	128918719
11	66729092	66729093	T		51	GENIC	homozygous	132155983
11	66730841	66730842	G	A	65	GENIC	homozygous	115888120