chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	11208254	11208255	A	G	26	GENIC	homozygous	110956585
17	11208810	11208811	T	G	27	GENIC	homozygous	110956587
17	11208988	11208989	G	T	43	GENIC	homozygous	110956589
17	11208998	11208999	G	A	46	GENIC	homozygous	110956591
17	11209061	11209062	C	A	42	GENIC	homozygous	110956593
17	11209107	11209108	G	A	39	GENIC	homozygous	110956595
17	11209234	11209235	T	C	49	GENIC	homozygous	110956597
17	11209393	11209394	T	C	34	GENIC	homozygous	110956599
17	11209463	11209464	T	C	28	GENIC	homozygous	110956601
17	11209723	11209724	A	G	29	GENIC	homozygous	110956603
17	11209851	11209852	A	T	38	GENIC	homozygous	110956605
17	11209958	11209959	G	A	60	GENIC	possibly homozygous	110956607
17	11210182	11210183	A	G	37	GENIC	possibly homozygous	110956609
17	11210218	11210219	G	A	33	GENIC	homozygous	110956611
17	11210416	11210417	G	C	41	GENIC	homozygous	110956613
17	11210426	11210427	T	A	39	GENIC	homozygous	110956615
17	11210427	11210428	C	T	40	GENIC	homozygous	110956617
17	11211098	11211099	C	T	33	GENIC	homozygous	110956619
17	11211241	11211242	C	T	35	GENIC	homozygous	110956622
17	11211494	11211495	C	T	37	GENIC	homozygous	110956624
17	11213024	11213025	G	A	34	GENIC	homozygous	110956626