chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	21051391	21051392	A	G	40	GENIC	homozygous	111753970
16	21060836	21060837	C	A	45	GENIC	possibly homozygous	111753972
16	21060929	21060930	A	G	44	GENIC	homozygous	111753974
16	21062196	21062197	G	T	19	GENIC	homozygous	111753978
16	21062494	21062495	A	T	39	GENIC	homozygous	111949218
16	21065493	21065494	G	A	40	GENIC	homozygous	111753982
16	21067463	21067464	T	C	45	GENIC	homozygous	111753987
16	21070282	21070283	G	A	43	GENIC	homozygous	111753989
16	21070358	21070359	A	G	50	GENIC	homozygous	111753991
16	21072368	21072369	C	T	51	GENIC	homozygous	111753993
16	21060811	21060812	A	G	50	GENIC	homozygous	112053066
16	21060912	21060913	G	T	46	GENIC	homozygous	112053067
16	21075790	21075791	C	A	47	GENIC	possibly homozygous	112053069
16	21076499	21076500	G	T	35	GENIC	homozygous	112053070
16	21057435	21057436	G	A	26	GENIC	homozygous	119099807
16	21061064	21061065	T	C	49	GENIC	homozygous	134747310
16	21061960	21061961	T	C	24	GENIC	homozygous	112401075
16	21064880	21064881	C	A	18	GENIC	homozygous	119146962
16	21072029	21072030	G	T	42	GENIC	homozygous	112150977
16	21073995	21073996	C	T	28	GENIC	homozygous	112434290
16	21074005	21074006	A	G	33	GENIC	homozygous	112320128