chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	3817487	3817488	T	G	47	GENIC	homozygous	112197961
16	3817547	3817548	G	A	48	GENIC	homozygous	112197963
16	3817588	3817589	G	A	47	GENIC	homozygous	112197965
16	3817705	3817706	T	G	37	GENIC	homozygous	112197967
16	3817782	3817783	C	T	35	GENIC	homozygous	112197969
16	3818016	3818016		GGGGGGGGGC	2	GENIC	homozygous	133029193
16	3818096	3818219	CTCGGAGGGATTTCTTTTTTTTTTTTTTTTTTTTTTCTATTCTTTTTTTTCGGAGCTGGGGATCGAACCCAGGGCCTTGCGCTTGCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAGCC		7	GENIC	homozygous	133029194
16	3818516	3818517	C	T	45	GENIC	homozygous	112197971
16	3819016	3819017	A	C	46	GENIC	homozygous	112197973
16	3819423	3819424	G	A	34	GENIC	homozygous	112197975
16	3819737	3819738	A	G	40	GENIC	homozygous	112197977
16	3819748	3819749	T	C	38	GENIC	homozygous	112197979
16	3819757	3819758	T	C	40	GENIC	homozygous	112197981
16	3819794	3819795	G	A	38	GENIC	homozygous	112197983
16	3819842	3819843	T	C	37	GENIC	homozygous	112197985
16	3819856	3819857	T		34	GENIC	homozygous	133029195
16	3819859	3819860	A	C	34	GENIC	homozygous	112197987
16	3819906	3819907	T	C	40	GENIC	homozygous	112197989
16	3819909	3819910	G	A	42	GENIC	homozygous	112197991
16	3820048	3820049	G	A	38	GENIC	homozygous	112197993
16	3820099	3820100	C	T	40	GENIC	homozygous	112197995
16	3820118	3820119	T	A	38	GENIC	homozygous	112197997
16	3820150	3820151	T	G	37	GENIC	homozygous	112197999
16	3820230	3820231	G	A	38	GENIC	homozygous	112198001
16	3820368	3820369	G	A	38	GENIC	homozygous	112198003
16	3820463	3820464	C	T	46	GENIC	possibly homozygous	112198005
16	3820635	3820636	T	C	51	GENIC	homozygous	112198007
16	3820739	3820740	T	C	49	GENIC	homozygous	112198009
16	3820886	3820887	T	C	41	GENIC	possibly homozygous	112198011