chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	225336016	225336017	A	G	12	GENIC	homozygous	110271378
2	225336376	225336377	G	C	33	GENIC	homozygous	110271384
2	225337207	225337208	T	C	27	GENIC	homozygous	110910637
2	225337270	225337271	C	T	17	GENIC	homozygous	111374873
2	225338692	225338693	G	T	14	GENIC	homozygous	110910638
2	225340445	225340446	C	T	27	GENIC	possibly homozygous	111374875
2	225342872	225342873	T	C	28	GENIC	homozygous	110271396
2	225349159	225349160	A	G	25	GENIC	homozygous	110271404
2	225340185	225340186	C	T	37	GENIC	homozygous	120217301
2	225349082	225349083	G	A	26	GENIC	homozygous	120217302
2	225344099	225344100	C	T	24	GENIC	homozygous	120131015
2	225344100	225344101	T	G	24	GENIC	homozygous	120131016
2	225357857	225357858	A	G	12	GENIC	homozygous	110271414
2	225358276	225358277	A	G	30	GENIC	homozygous	110271416
2	225360728	225360729	A	C	24	GENIC	homozygous	120217303
2	225363202	225363203	A	T	39	GENIC	homozygous	120217304
2	225367686	225367687	A	G	26	GENIC	homozygous	110271432
2	225368407	225368408	T	G	38	GENIC	homozygous	110271434
2	225368996	225368997	C	G	36	GENIC	homozygous	120217305
2	225375150	225375151	G	A	29	GENIC	homozygous	120217306
2	225385193	225385194	G	T	32	GENIC	homozygous	120217307
2	225388523	225388524	C	T	28	GENIC	homozygous	120217308