chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	264267005	264267006	T	C	17	GENIC	homozygous	110441279
2	264267027	264267028	T	G	14	GENIC	heterozygous	120259130
2	264267132	264267133	A	G	17	GENIC	homozygous	110441280
2	264267409	264267410	C	T	29	GENIC	homozygous	110441281
2	264267550	264267551	T	C	25	GENIC	homozygous	110441283
2	264267826	264267827	C	T	32	GENIC	homozygous	110441284
2	264267972	264267973	A	G	31	GENIC	homozygous	120132768
2	264268003	264268004	A	G	34	GENIC	homozygous	110441285
2	264268784	264268785	C	T	23	GENIC	homozygous	110441286
2	264269097	264269098	G	A	35	GENIC	homozygous	110441287
2	264269700	264269701	A	G	29	GENIC	homozygous	110441288
2	264271106	264271107	T	C	30	GENIC	homozygous	110441289
2	264271201	264271202	A	G	35	GENIC	homozygous	110441290
2	264271700	264271701	C	T	29	GENIC	homozygous	110441291
2	264272433	264272434	A	G	20	GENIC	homozygous	110441294
2	264272675	264272676	T	C	20	GENIC	homozygous	110441295
2	264273650	264273651	A	C	24	GENIC	homozygous	110441298
2	264273927	264273928	T	A	19	GENIC	homozygous	110441299
2	264274250	264274251	T	C	29	GENIC	homozygous	110441300
2	264274547	264274548	A	T	18	GENIC	homozygous	110441301
2	264274717	264274718	T	C	27	GENIC	homozygous	110441302