chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	228686468	228686469	C	T	31	GENIC	homozygous	120877175
1	228686590	228686591	A	G	48	GENIC	homozygous	109001392
1	228686868	228686869	C	T	39	GENIC	homozygous	109001394
1	228687326	228687327	A	G	30	GENIC	homozygous	120877176
1	228687552	228687553	G	A	32	GENIC	homozygous	120877177
1	228687921	228687922	A	G	37	GENIC	homozygous	120877178
1	228688171	228688172	C	A	30	GENIC	homozygous	120877179
1	228688374	228688375	C	T	33	GENIC	homozygous	109001396
1	228688379	228688380	T	A	34	GENIC	homozygous	120877180
1	228688448	228688449	C	T	33	GENIC	homozygous	120877181
1	228689209	228689210	G	A	41	GENIC	homozygous	120877182
1	228689303	228689304	G	T	33	GENIC	homozygous	120877183
1	228689907	228689908	G	C	26	GENIC	homozygous	109001399
1	228690502	228690503	A	G	28	GENIC	homozygous	109001400
1	228691357	228691358	C	T	29	GENIC	homozygous	120877184
1	228691372	228691373	T	C	30	GENIC	homozygous	120877185
1	228691391	228691392	C	A	28	GENIC	homozygous	109001401
1	228692276	228692277	G	C	27	GENIC	homozygous	120877186
1	228692432	228692433	T	C	27	GENIC	homozygous	109001403
1	228692514	228692515	G	A	22	GENIC	homozygous	120877187
1	228692575	228692576	G	A	30	GENIC	homozygous	120877188