chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	1550373	1550374	T	G	39	GENIC	possibly homozygous	111920888
16	1551763	1551764	A	G	59	GENIC	homozygous	111920890
16	1553323	1553324	A	G	54	GENIC	homozygous	112194639
16	1553419	1553420	A	G	54	GENIC	homozygous	111920892
16	1553605	1553606	A	G	61	GENIC	homozygous	111920894
16	1553955	1553956	T	C	57	GENIC	homozygous	111920897
16	1554851	1554852	C	T	51	GENIC	homozygous	111920899
16	1555722	1555723	C	T	44	GENIC	possibly homozygous	111920901
16	1556595	1556596	T	C	56	GENIC	possibly homozygous	111920903
16	1556659	1556660	T	C	54	GENIC	possibly homozygous	111920905
16	1556841	1556842	T	C	53	GENIC	homozygous	111920907
16	1557331	1557332	A	G	54	GENIC	homozygous	111920909
16	1557678	1557679	A	G	40	GENIC	homozygous	111920911
16	1558373	1558374	T	C	39	GENIC	homozygous	111920913
16	1554165	1554165		GG	31	GENIC	homozygous	131170982