chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	88148268	88148269	C	T	63	GENIC	possibly homozygous	115929853
11	88148494	88148495	T	C	57	GENIC	homozygous	115929855
11	88149074	88149082	TGTGTGTC		74	GENIC	homozygous	128931928
11	88149146	88149147	C	T	63	GENIC	homozygous	115929857
11	88149719	88149720	G	A	48	GENIC	homozygous	115929859
11	88149752	88149753	G	A	49	GENIC	homozygous	115929861
11	88149769	88149770	T		42	GENIC	possibly homozygous	128931929
11	88150211	88150212	G		18	GENIC	possibly homozygous	128931930
11	88152107	88152107		CTGCTG	45	GENIC	homozygous	128931931
11	88152184	88152185	T	C	49	GENIC	homozygous	115929863
11	88152978	88152979	G	T	42	GENIC	homozygous	115929865
11	88153566	88153566		T	24	GENIC	possibly homozygous	128931932
11	88154625	88154626	C	T	56	GENIC	homozygous	115929867
11	88157880	88157881	A	G	62	GENIC	homozygous	115929869
11	88161582	88161592	AAATCCCTGA		59	GENIC	homozygous	128931933
11	88162745	88162746	C	T	48	GENIC	homozygous	115929871
11	88166027	88166028	A	C	62	GENIC	homozygous	115929873
11	88169151	88169152	G	A	64	GENIC	homozygous	115929876
11	88166365	88166366	G	A	49	GENIC	homozygous	116359113