chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
17	30617663	30617664	T	C	11	GENIC	homozygous	111023208
17	30618384	30618385	A	G	13	GENIC	homozygous	111023210
17	30621425	30621426	C	T	18	GENIC	homozygous	111023212
17	30621759	30621760	C	A	26	GENIC	homozygous	111023214
17	30623737	30623738	T	C	16	GENIC	homozygous	111023216
17	30625321	30625322	C	T	13	GENIC	homozygous	111023218
17	30625942	30625943	A	G	53	GENIC	heterozygous	119272533
17	30625976	30625977	C	T	39	GENIC	heterozygous	119272535
17	30625989	30625990	T	C	44	GENIC	heterozygous	119272536
17	30626317	30626318	G	T	21	GENIC	heterozygous	119272538
17	30626873	30626874	A	G	35	GENIC	heterozygous	119272539
17	30626979	30626980	G	A	28	GENIC	heterozygous	111386640
17	30630041	30630042	A	G	24	GENIC	homozygous	111023220
17	30632466	30632467	C	T	28	GENIC	possibly homozygous	119272541
17	30634511	30634512	A	G	35	GENIC	heterozygous	119272545
17	30634605	30634606	T	C	28	GENIC	heterozygous	119272547
17	30635127	30635128	G	A	19	GENIC	heterozygous	119272549
17	30635288	30635289	A	G	47	GENIC	possibly homozygous	119272550
17	30635376	30635377	C	A	34	GENIC	heterozygous	119423338
17	30635427	30635428	C	T	39	GENIC	heterozygous	119423340
17	30635430	30635431	C	G	39	GENIC	heterozygous	119423342