chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	10556040	10556041	T	C	43	GENIC	homozygous	111933391
16	10556427	10556428	G	C	19	GENIC	homozygous	111723840
16	10556812	10556813	A	G	25	GENIC	homozygous	111933393
16	10557957	10557958	G	A	25	GENIC	homozygous	111723844
16	10558844	10558845	A	G	25	GENIC	homozygous	111933395
16	10559105	10559106	G	A	28	GENIC	homozygous	111933397
16	10559605	10559606	A	G	10	GENIC	homozygous	111933403
16	10559693	10559694	T	G	12	GENIC	homozygous	111933405
16	10560336	10560337	C	T	24	GENIC	homozygous	111933407
16	10560831	10560832	G	C	21	GENIC	homozygous	111933409
16	10563526	10563527	A	G	11	GENIC	homozygous	111723848
16	10564639	10564640	T	C	21	GENIC	homozygous	111723850
16	10557221	10557222	G	A	37	GENIC	possibly homozygous	112400517
16	10559897	10559898	C	A	15	GENIC	possibly homozygous	112400518
16	10559915	10559916	T	G	17	GENIC	possibly homozygous	112400519
16	10561016	10561017	T	C	25	GENIC	homozygous	112400520