chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10277802	10277803	A	G	57	GENIC	homozygous	111722582
16	10278626	10278627	A	G	52	GENIC	homozygous	111722584
16	10279376	10279377	T	G	54	GENIC	homozygous	111722586
16	10279967	10279968	G	A	53	GENIC	homozygous	111722588
16	10280217	10280218	G	A	41	GENIC	homozygous	111722590
16	10280471	10280472	C	A	44	GENIC	homozygous	111722592
16	10280950	10280951	G	A	52	GENIC	homozygous	111722594
16	10281572	10281573	G	A	48	GENIC	homozygous	111722596
16	10281700	10281701	G	A	52	GENIC	homozygous	111722599
16	10281930	10281931	A	T	54	GENIC	homozygous	111722601
16	10282011	10282012	G	T	56	GENIC	homozygous	111722603
16	10282172	10282173	A	G	67	GENIC	homozygous	111722605
16	10282214	10282215	A	G	65	GENIC	homozygous	111722607
16	10282930	10282931	G	A	59	GENIC	homozygous	111722609
16	10282949	10282950	C	T	47	GENIC	homozygous	111722611
16	10283022	10283023	A	T	43	GENIC	homozygous	111933058
16	10283027	10283028	A	C	47	GENIC	possibly homozygous	111933060
16	10283333	10283334	G	A	45	GENIC	homozygous	111722615
16	10283351	10283352	G	A	46	GENIC	homozygous	111722617
16	10283402	10283403	C	T	61	GENIC	homozygous	111722619
16	10283460	10283461	C	A	63	GENIC	homozygous	111722621
16	10283685	10283686	A	G	67	GENIC	homozygous	111722623
16	10283885	10283886	A	G	66	GENIC	possibly homozygous	111722625
16	10283896	10283897	C	T	71	GENIC	homozygous	111722627
16	10283994	10283995	G	A	58	GENIC	homozygous	111722629
16	10284006	10284007	T	C	63	GENIC	homozygous	111722631
16	10284090	10284091	C	T	54	GENIC	homozygous	111722633
16	10284571	10284572	C	T	51	GENIC	homozygous	111722635
16	10284910	10284911	C	T	64	GENIC	homozygous	111722637
16	10285348	10285349	A	G	71	GENIC	homozygous	111722639
16	10285542	10285543	C	T	52	GENIC	homozygous	111722641
16	10286078	10286079	C	T	51	GENIC	homozygous	111722643
16	10286240	10286241	G	A	49	GENIC	homozygous	111722645