chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55517204	55517205	C	A	14	GENIC	possibly homozygous	52058564
10	55517307	55517308	A	G	19	GENIC	possibly homozygous	51459719
10	55517464	55517465	A	G	17	GENIC	homozygous	51459720
10	55518157	55518158	A	G	12	GENIC	possibly homozygous	51459721
10	55518219	55518220	C	CG	9	GENIC	possibly homozygous	51459722
10	55518236	55518237	G	A	3	GENIC	homozygous	51459723
10	55518755	55518763	GGTAGCCG	--------	2	GENIC	homozygous	52058566
10	55518776	55518777	T	C	9	GENIC	homozygous	51459724
10	55518887	55518888	C	T	15	GENIC	possibly homozygous	51459725
10	55519667	55519668	G	A	13	GENIC	possibly homozygous	51459728
10	55520400	55520401	A	G	3	GENIC	homozygous	51459729
10	55520858	55520859	C	T	21	GENIC	homozygous	52058572
10	55521191	55521192	G	A	15	GENIC	homozygous	51459730
10	55521577	55521578	A	G	12	GENIC	possibly homozygous	51459731
10	55521834	55521835	C	T	18	GENIC	homozygous	51459732
10	55521879	55521880	C	T	13	GENIC	homozygous	52058574
10	55521958	55521959	G	A	17	GENIC	homozygous	51459733
10	55523036	55523037	G	T	5	GENIC	heterozygous	51459739
10	55523128	55523129	T	C	16	GENIC	homozygous	51459740
10	55523747	55523748	C	CA	2	GENIC	homozygous	51653097
10	55523762	55523763	T	G	5	GENIC	homozygous	51459742
10	55524656	55524657	T	C	6	GENIC	homozygous	51459744
10	55524928	55524929	T	C	18	GENIC	possibly homozygous	51459746