chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	225334953	225334954	G	A	54	GENIC	homozygous	61101598
1	225336160	225336161	G	-	11	GENIC	homozygous	61101599
1	225336714	225336715	T	C	60	GENIC	homozygous	61101600
1	225336926	225336927	C	T	55	GENIC	possibly homozygous	61101601
1	225337097	225337098	C	G	54	GENIC	homozygous	61101602
1	225337563	225337564	G	A	70	GENIC	homozygous	61101603
1	225338283	225338284	G	T	66	GENIC	heterozygous	61321542
1	225338304	225338305	G	T	65	GENIC	heterozygous	61321543
1	225338307	225338308	A	G	59	GENIC	heterozygous	61321544
1	225338515	225338516	G	A	38	GENIC	homozygous	61101605
1	225338634	225338638	TTTT	----	46	GENIC	homozygous	61101606
1	225338809	225338810	T	G	40	GENIC	homozygous	61101607
1	225338996	225338997	A	G	34	GENIC	homozygous	61101608
1	225339538	225339539	A	T	80	GENIC	possibly homozygous	61101609
1	225339553	225339554	C	CAGAG	57	GENIC	possibly homozygous	61101610
1	225339685	225339686	A	G	54	GENIC	homozygous	61101611
1	225339823	225339843	TTTCTTTTCTTTTCTTTTCT	--------------------	8	GENIC	homozygous	61101612
1	225339842	225339843	T	-	40	GENIC	heterozygous	61101613
1	225340596	225340597	A	-	41	GENIC	homozygous	61101615
1	225341293	225341294	T	A	65	GENIC	possibly homozygous	61101616
1	225341505	225341506	G	GTGTGTGT	28	GENIC	heterozygous	61101617
1	225341505	225341506	G	GGT	28	GENIC	possibly homozygous	61101618
1	225343981	225343982	C	A	68	GENIC	possibly homozygous	61101619