chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	20653160	20653161	T	C	26	GENIC	homozygous	111753188
16	20654893	20654894	A	G	31	GENIC	possibly homozygous	111753192
16	20658183	20658184	C	T	18	GENIC	homozygous	112150908
16	20658902	20658903	A	T	19	GENIC	homozygous	111753198
16	20659271	20659272	G	A	32	GENIC	possibly homozygous	112150910
16	20660159	20660160	A	G	36	GENIC	possibly homozygous	111753200
16	20661266	20661267	G	C	16	GENIC	homozygous	112150912
16	20661296	20661297	G	A	28	GENIC	possibly homozygous	112150914
16	20662009	20662010	A	T	28	GENIC	possibly homozygous	112150916
16	20662010	20662011	G	T	28	GENIC	possibly homozygous	112150918
16	20662548	20662549	C	T	31	GENIC	possibly homozygous	112150920
16	20665657	20665658	T	C	36	GENIC	possibly homozygous	111753208
16	20665670	20665671	C	G	38	GENIC	possibly homozygous	112150922
16	20666270	20666271	T	A	30	GENIC	possibly homozygous	112150924