chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	23202753	23202754	G	A	10	GENIC	homozygous	142536992
16	23203592	23203593	A	G	12	GENIC	homozygous	142536993
16	23203667	23203668	G	A	13	GENIC	homozygous	142536994
16	23203942	23203943	G	A	9	GENIC	homozygous	139899079
16	23204104	23204105	T	C	8	GENIC	homozygous	139899080
16	23204602	23204603	A	C	9	GENIC	homozygous	142536995
16	23204650	23204651	A	G	6	GENIC	homozygous	139899081
16	23204816	23204817	C	T	14	GENIC	homozygous	139899082
16	23204850	23204850		CTTT	13	GENIC	homozygous	139826725
16	23205952	23205953	C	T	12	GENIC	homozygous	142536996
16	23205958	23205958		A	12	GENIC	homozygous	139826726
16	23206910	23206911	A	C	14	GENIC	homozygous	139899083
16	23207964	23207965	A	G	14	GENIC	homozygous	139899084
16	23208035	23208036	T	C	15	GENIC	possibly homozygous	139899085
16	23208824	23208825	G	T	12	GENIC	homozygous	139899087
16	23209142	23209143	G	C	20	GENIC	homozygous	139899088
16	23209572	23209573	G	A	21	GENIC	homozygous	142536997