chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	26624165	26624166	A	G	63	GENIC	homozygous	140088625
17	26628731	26628732	G	A	50	GENIC	homozygous	140088626
17	26629362	26629363	G	A	65	GENIC	homozygous	140088628
17	26629580	26629581	G	A	47	GENIC	homozygous	140088629
17	26629604	26629605	A	T	49	GENIC	homozygous	140088630
17	26630918	26630919	T	A	37	GENIC	homozygous	140088631
17	26631909	26631910	C	T	58	GENIC	homozygous	142597865
17	26631995	26631996	C	T	56	GENIC	homozygous	140088632
17	26632592	26632593	G	T	47	GENIC	heterozygous	155007946
17	26632592	26632593	G		47	GENIC	heterozygous	403411156
17	26632596	26632597	G	T	47	GENIC	possibly homozygous	155007947
17	26632596	26632597	G		47	GENIC	heterozygous	403411157
17	26632600	26632601	G	T	45	GENIC	homozygous	142597866
17	26634857	26634858	A	G	67	GENIC	homozygous	140088633
17	26636321	26636322	A	G	65	GENIC	homozygous	140088634
17	26638450	26638451	T	A	47	GENIC	homozygous	140088635
17	26640516	26640517	G	A	68	GENIC	homozygous	142597867
17	26640530	26640531	G	C	75	GENIC	homozygous	142597868
17	26648324	26648325	A	G	57	GENIC	homozygous	140088649
17	26632627	26632627		T	52	GENIC	homozygous	140017152