chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	49297877	49297878	G	C	25	GENIC	homozygous	962385201
16	49297880	49297881	C	G	25	GENIC	homozygous	962385202
16	49297901	49297902	C	A	30	GENIC	homozygous	962385203
16	49297949	49297950	G	A	30	GENIC	homozygous	962385204
16	49298498	49298499	C	G	19	GENIC	homozygous	962385205
16	49300595	49300596	G	A	30	GENIC	homozygous	962385206
16	49310356	49310357	A	G	33	GENIC	homozygous	962385207
16	49316984	49316985	G	A	34	GENIC	homozygous	962385208
16	49321001	49321002	T	C	38	GENIC	homozygous	962385209
16	49321341	49321342	T	C	21	GENIC	homozygous	962385210
16	49322929	49322930	C	T	22	GENIC	homozygous	962385211
16	49323114	49323115	G	A	41	GENIC	homozygous	962385212
16	49323222	49323223	A	T	35	GENIC	homozygous	962385213
16	49323305	49323306	C	T	24	GENIC	homozygous	962385214
16	49325269	49325270	T	C	27	GENIC	homozygous	962385215
16	49326197	49326198	T	C	48	GENIC	homozygous	962385216
16	49328078	49328079	T	C	34	GENIC	homozygous	962385217