chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	228397652	228397653	C	A	18	GENIC	homozygous	109000687
1	228399575	228399576	T	C	9	GENIC	homozygous	109000694
1	228400034	228400035	C	T	14	GENIC	homozygous	120491651
1	228400111	228400112	C	T	16	GENIC	homozygous	109000698
1	228401400	228401401	C	A	13	GENIC	homozygous	109000699
1	228402799	228402800	T	C	8	GENIC	homozygous	109000700
1	228403946	228403947	C	T	12	GENIC	homozygous	120491652
1	228405898	228405899	A	G	12	GENIC	homozygous	109000701
1	228406349	228406350	A	G	12	GENIC	homozygous	109000702
1	228409320	228409321	G	A	13	GENIC	homozygous	120491653
1	228409509	228409510	A	G	11	GENIC	homozygous	109000706
1	228413607	228413608	C	T	11	GENIC	homozygous	109000708
1	228413730	228413731	T	A	8	GENIC	homozygous	109000711
1	228414335	228414336	T	G	7	GENIC	homozygous	109000712
1	228418405	228418406	A	G	11	GENIC	homozygous	120491654
1	228421171	228421172	A	G	4	GENIC	homozygous	109000716
1	228422783	228422784	G	A	10	GENIC	homozygous	109000719