chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	41883565	41883566	T	C	21	GENIC	homozygous	154696286
11	41883573	41883573		G	20	GENIC	homozygous	138886116
11	41884548	41884549	C	T	52	GENIC	homozygous	138979830
11	41884230	41884231	A	T	46	GENIC	possibly homozygous	143500756
11	41884449	41884450	T	G	41	GENIC	homozygous	143500757
11	41884561	41884562	C	G	53	GENIC	homozygous	138979831
11	41884568	41884569	A	G	53	GENIC	homozygous	138979832
11	41884599	41884600	T	C	50	GENIC	homozygous	138979833
11	41885037	41885038	G	A	39	GENIC	homozygous	143500758
11	41885464	41885465	A	C	57	GENIC	homozygous	143500759
11	41886237	41886238	C	T	48	GENIC	homozygous	143500760
11	41886270	41886271	G	A	48	GENIC	homozygous	143500761
11	41886368	41886369	C	T	41	GENIC	homozygous	143500762
11	41886442	41886443	T	C	39	GENIC	homozygous	143500763
11	41886817	41886818	C	T	56	GENIC	homozygous	143500764
11	41886905	41886906	G	A	67	GENIC	homozygous	143500765
11	41887009	41887010	A	G	54	GENIC	homozygous	143500766
11	41887177	41887178	T	A	46	GENIC	homozygous	143500767
11	41887391	41887392	G	A	40	GENIC	homozygous	154696288
11	41887449	41887450	T	C	52	GENIC	homozygous	143500768
11	41887833	41887834	G	A	51	GENIC	homozygous	143500769
11	41888037	41888038	T	G	46	GENIC	homozygous	143500770
11	41889330	41889331	A	C	39	GENIC	homozygous	138979836
11	41888404	41888404		TAAA	35	GENIC	homozygous	143476898
11	41887391	41887392	G		40	GENIC	heterozygous	403304770