chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	23202472	23202473	T	C	10	GENIC	homozygous	139899072
16	23202629	23202630	G	A	35	GENIC	homozygous	139899073
16	23202647	23202648	C	T	30	GENIC	homozygous	139899074
16	23202692	23202693	C	T	32	GENIC	homozygous	139899075
16	23202849	23202850	T	G	37	GENIC	homozygous	139899076
16	23203092	23203093	T	C	50	GENIC	homozygous	139899077
16	23203804	23203805	C	A	32	GENIC	homozygous	139899078
16	23203942	23203943	G	A	28	GENIC	homozygous	139899079
16	23204104	23204105	T	C	11	GENIC	homozygous	139899080
16	23204650	23204651	A	G	26	GENIC	homozygous	139899081
16	23204816	23204817	C	T	34	GENIC	homozygous	139899082
16	23203621	23203621		C	39	GENIC	homozygous	139826724
16	23204850	23204850		CTTT	40	GENIC	homozygous	139826725
16	23205958	23205958		A	50	GENIC	homozygous	139826726
16	23206910	23206911	A	C	32	GENIC	homozygous	139899083
16	23207643	23207643		T	42	GENIC	possibly homozygous	139826727
16	23207964	23207965	A	G	43	GENIC	homozygous	139899084
16	23208035	23208036	T	C	52	GENIC	homozygous	139899085
16	23208080	23208081	G	A	53	GENIC	homozygous	139899086
16	23208824	23208825	G	T	46	GENIC	homozygous	139899087
16	23209142	23209143	G	C	34	GENIC	homozygous	139899088