chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	56248391	56248392	T	C	12	GENIC	homozygous	111830098
16	56250048	56250049	T	A	25	GENIC	homozygous	111830100
16	56250197	56250198	T	C	23	GENIC	homozygous	111830102
16	56250203	56250204	G	C	22	GENIC	homozygous	111830104
16	56250428	56250429	G	C	34	GENIC	possibly homozygous	111830106
16	56250611	56250612	T	C	17	GENIC	homozygous	111830108
16	56265226	56265227	C	T	31	GENIC	possibly homozygous	111830111
16	56278723	56278724	T	C	29	GENIC	homozygous	111830113
16	56287052	56287053	C	T	16	GENIC	homozygous	111830115
16	56287879	56287880	T	A	19	GENIC	homozygous	111830117
16	56287928	56287929	G	T	23	GENIC	homozygous	111989069
16	56293295	56293296	A	G	19	GENIC	homozygous	111830119
16	56293718	56293719	A	C	18	GENIC	homozygous	111830121
16	56293731	56293732	T	G	17	GENIC	homozygous	111989111
16	56294896	56294897	T	C	29	GENIC	possibly homozygous	111830123
16	56299946	56299947	A	G	28	GENIC	possibly homozygous	111830125
16	56300626	56300627	T	C	48	GENIC	homozygous	111830127
16	56359109	56359110	A	G	18	GENIC	possibly homozygous	111830133
16	56359274	56359275	A	G	30	GENIC	possibly homozygous	111830135
16	56361235	56361236	C	T	28	GENIC	homozygous	111830137
16	56372119	56372120	G	A	27	GENIC	homozygous	111830139
16	56392844	56392845	G	A	16	GENIC	possibly homozygous	111830143