chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	90014780	90014781	T	TCCC	9	GENIC	homozygous	51203815
11	90014790	90014791	C	CGT	3	GENIC	homozygous	51203817
11	90015272	90015273	A	G	23	GENIC	homozygous	51034982
11	90016508	90016509	T	-	26	GENIC	homozygous	51034984
11	90016539	90016540	T	-	24	GENIC	homozygous	51203819
11	90016895	90016896	G	A	26	GENIC	homozygous	51203822
11	90016904	90016905	A	G	31	GENIC	homozygous	51203824
11	90017214	90017215	G	A	40	GENIC	homozygous	51134596
11	90015316	90015317	G	A	20	GENIC	homozygous	51134590
11	90015317	90015318	C	A	20	GENIC	homozygous	51134593
11	90017589	90017590	G	C	36	GENIC	homozygous	51034987
11	90017993	90017994	A	T	29	GENIC	homozygous	51034988
11	90019442	90019443	A	G	39	GENIC	homozygous	51034991
11	90020577	90020578	C	A	16	GENIC	homozygous	51203826
11	90020624	90020625	A	C	19	GENIC	homozygous	51034993