chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	228396792	228396793	C	T	17	GENIC	homozygous	109000685
1	228397127	228397128	C	T	25	GENIC	homozygous	109000686
1	228397652	228397653	C	A	15	GENIC	homozygous	109000687
1	228397916	228397917	T	C	13	GENIC	homozygous	109000688
1	228398595	228398596	T	C	19	GENIC	homozygous	109000689
1	228398920	228398921	C	T	19	GENIC	homozygous	109000690
1	228399190	228399191	G	A	27	GENIC	homozygous	109000691
1	228399421	228399422	C	T	22	GENIC	homozygous	109000692
1	228399556	228399557	T	A	16	GENIC	homozygous	109000693
1	228399575	228399576	T	C	14	GENIC	homozygous	109000694
1	228399576	228399577	G	A	14	GENIC	homozygous	109000695
1	228399714	228399715	T	C	14	GENIC	homozygous	109000696
1	228399964	228399965	A	G	21	GENIC	homozygous	109000697
1	228400111	228400112	C	T	24	GENIC	homozygous	109000698
1	228401400	228401401	C	A	17	GENIC	homozygous	109000699
1	228402799	228402800	T	C	6	GENIC	homozygous	109000700
1	228405898	228405899	A	G	23	GENIC	homozygous	109000701
1	228406349	228406350	A	G	24	GENIC	homozygous	109000702
1	228408015	228408016	C	G	28	GENIC	homozygous	109000703
1	228409233	228409234	G	T	36	GENIC	homozygous	109000704
1	228409429	228409430	G	A	22	GENIC	homozygous	109000705
1	228409509	228409510	A	G	19	GENIC	homozygous	109000706
1	228413583	228413584	A	G	13	GENIC	homozygous	109000707
1	228413607	228413608	C	T	17	GENIC	homozygous	109000708
1	228413620	228413621	C	T	19	GENIC	homozygous	109000709
1	228413631	228413632	T	C	19	GENIC	homozygous	109000710
1	228413730	228413731	T	A	13	GENIC	homozygous	109000711
1	228414335	228414336	T	G	20	GENIC	homozygous	109000712
1	228415875	228415876	T	A	37	GENIC	homozygous	109000713
1	228416674	228416675	T	C	11	GENIC	homozygous	109000714
1	228419750	228419751	G	T	19	GENIC	homozygous	109000715
1	228421293	228421294	C	T	17	GENIC	homozygous	109000717
1	228421301	228421302	T	G	19	GENIC	homozygous	109000718
1	228422783	228422784	G	A	25	GENIC	homozygous	109000719
1	228424056	228424057	T	G	24	GENIC	homozygous	109000720