chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	3836083	3836084	C	CA	32	GENIC	homozygous	47248435
16	3853977	3853978	C	G	27	GENIC	possibly homozygous	47248436
16	3863661	3863662	T	A	16	GENIC	homozygous	47248437
16	3863664	3863665	T	A	20	GENIC	possibly homozygous	47248438
16	3863667	3863668	T	A	18	GENIC	possibly homozygous	47248439
16	3864766	3864770	TCTC	----	5	GENIC	heterozygous	47248440
16	3864768	3864770	TC	--	5	GENIC	heterozygous	47248441
16	3867477	3867478	A	G	55	GENIC	heterozygous	47248442
16	3867758	3867759	A	C	30	GENIC	homozygous	47248443
16	3867759	3867760	T	C	29	GENIC	homozygous	47248444
16	3868376	3868377	G	GA	33	GENIC	heterozygous	47248445
16	3869060	3869061	C	CCAGTG	2	GENIC	homozygous	47248446
16	3871551	3871555	TATC	----	22	GENIC	possibly homozygous	47248447
16	3871756	3871757	G	A	49	GENIC	heterozygous	47248448
16	3871764	3871765	A	G	48	GENIC	heterozygous	47248449
16	3871764	3871765	A	ATATGTATG	29	GENIC	homozygous	47248450
16	3871780	3871781	C	G	44	GENIC	heterozygous	47248451
16	3871784	3871785	C	G	46	GENIC	heterozygous	47248452
16	3871936	3871937	C	G	45	GENIC	possibly homozygous	47248453
16	3876208	3876210	AC	--	17	GENIC	heterozygous	47248454