chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55517204	55517205	C	G	15	GENIC	homozygous	51459718
10	55517307	55517308	A	G	21	GENIC	homozygous	51459719
10	55517464	55517465	A	G	11	GENIC	homozygous	51459720
10	55518157	55518158	A	G	20	GENIC	possibly homozygous	51459721
10	55518219	55518220	C	CG	16	GENIC	heterozygous	51459722
10	55518236	55518237	G	A	15	GENIC	homozygous	51459723
10	55518776	55518777	T	C	17	GENIC	homozygous	51459724
10	55518887	55518888	C	T	24	GENIC	possibly homozygous	51459725
10	55519108	55519109	T	A	16	GENIC	possibly homozygous	51459726
10	55519247	55519248	C	G	12	GENIC	heterozygous	51459727
10	55519667	55519668	G	A	14	GENIC	homozygous	51459728
10	55520400	55520401	A	G	11	GENIC	possibly homozygous	51459729
10	55521191	55521192	G	A	14	GENIC	homozygous	51459730
10	55521577	55521578	A	G	11	GENIC	homozygous	51459731
10	55521834	55521835	C	T	27	GENIC	homozygous	51459732
10	55521958	55521959	G	A	26	GENIC	possibly homozygous	51459733
10	55522763	55522764	A	C	2	GENIC	homozygous	51459734
10	55522876	55522877	G	C	10	GENIC	homozygous	51459738
10	55523036	55523037	G	T	9	GENIC	possibly homozygous	51459739
10	55523128	55523129	T	C	19	GENIC	homozygous	51459740
10	55523748	55523749	A	-	2	GENIC	homozygous	51459741
10	55523762	55523763	T	G	6	GENIC	homozygous	51459742
10	55524541	55524542	G	A	25	GENIC	homozygous	51459743
10	55524656	55524657	T	C	9	GENIC	possibly homozygous	51459744
10	55524928	55524929	T	C	14	GENIC	heterozygous	51459746
10	55525761	55525762	C	T	15	GENIC	homozygous	51459747
10	55525776	55525777	G	C	11	GENIC	possibly homozygous	51459748