chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	1731081	1731082	T	C	63	GENIC	possibly homozygous	110937125
17	1749752	1749753	C	T	52	GENIC	homozygous	110937128
17	1749758	1749759	C	A	41	GENIC	possibly homozygous	110937130
17	1749760	1749761	G	A	40	GENIC	homozygous	110937133
17	1749763	1749764	C	A	41	GENIC	homozygous	110937135
17	1749768	1749769	C	T	44	GENIC	homozygous	110937138
17	1756384	1756385	A	G	64	GENIC	heterozygous	119322475
17	1756421	1756422	T	C	85	GENIC	heterozygous	119260715
17	1756445	1756446	T	G	141	GENIC	heterozygous	119260716
17	1756593	1756594	A	G	137	GENIC	heterozygous	119322476
17	1757317	1757318	T	C	46	GENIC	heterozygous	119322477
17	1757336	1757337	C	A	69	GENIC	heterozygous	119322478
17	1757406	1757407	G	A	119	GENIC	heterozygous	119260717
17	1758034	1758035	A	G	123	GENIC	heterozygous	119260718
17	1758146	1758147	G	A	99	GENIC	heterozygous	119260719
17	1766975	1766976	G	A	24	GENIC	possibly homozygous	119260720
17	1778509	1778510	G	T	19	GENIC	homozygous	119260721
17	1780071	1780072	C	T	34	GENIC	heterozygous	119322479
17	1797139	1797140	T	G	27	GENIC	homozygous	111479259