chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	56224627	56224628	T	-	13	GENIC	possibly homozygous	47142528
17	56224777	56224778	G	A	15	GENIC	possibly homozygous	47142529
17	56224940	56224941	C	T	10	GENIC	homozygous	47142530
17	56225002	56225003	A	AC	4	GENIC	homozygous	47142531
17	56225053	56225054	C	A	12	GENIC	homozygous	47142532
17	56225255	56225256	G	T	9	GENIC	homozygous	47142533
17	56228537	56228538	T	C	7	GENIC	homozygous	47142534
17	56228592	56228593	G	A	25	GENIC	homozygous	47142535
17	56229139	56229140	G	A	13	GENIC	homozygous	47142537
17	56229449	56229450	C	T	15	GENIC	homozygous	47142538
17	56229708	56229709	T	C	2	GENIC	homozygous	47142542
17	56229824	56229825	G	C	7	GENIC	possibly homozygous	47142543
17	56229848	56229849	G	GGGA	5	GENIC	homozygous	47142544
17	56229996	56229997	C	T	9	GENIC	homozygous	47142545
17	56232129	56232130	C	T	13	GENIC	homozygous	47142548
17	56232696	56232697	A	AT	6	GENIC	heterozygous	47142549
17	56236521	56236522	G	A	16	GENIC	homozygous	47142551
17	56236538	56236539	A	T	14	GENIC	homozygous	47142552
17	56237258	56237259	G	A	20	GENIC	homozygous	47142553
17	56240254	56240255	G	A	13	GENIC	homozygous	47142556