chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21051391	21051392	A	G	51	GENIC	homozygous	111753970
16	21060836	21060837	C	A	39	GENIC	homozygous	111753972
16	21060929	21060930	A	G	56	GENIC	homozygous	111753974
16	21061671	21061672	T	C	41	GENIC	homozygous	111753976
16	21062196	21062197	G	T	29	GENIC	homozygous	111753978
16	21062494	21062495	A	T	47	GENIC	homozygous	111949218
16	21063646	21063647	G	A	57	GENIC	homozygous	111753980
16	21065493	21065494	G	A	47	GENIC	homozygous	111753982
16	21067463	21067464	T	C	49	GENIC	homozygous	111753987
16	21070282	21070283	G	A	53	GENIC	possibly homozygous	111753989
16	21070358	21070359	A	G	52	GENIC	possibly homozygous	111753991
16	21072368	21072369	C	T	61	GENIC	homozygous	111753993
16	21073995	21073996	C	T	27	GENIC	homozygous	112434290
16	21074005	21074006	A	G	29	GENIC	homozygous	112320128
16	21057435	21057436	G	A	25	GENIC	homozygous	119099807
16	21064855	21064856	C	T	22	GENIC	homozygous	119099808
16	21064880	21064881	C	A	19	GENIC	homozygous	119146962
16	21072029	21072030	G	T	35	GENIC	homozygous	112150977