chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	50714148	50714149	C	T	14	GENIC	homozygous	117540568
9	50715924	50715925	C	T	25	GENIC	homozygous	117335020
9	50716908	50716909	G	A	25	GENIC	homozygous	117540570
9	50719266	50719267	T	C	24	GENIC	homozygous	117540572
9	50725234	50725235	G	T	27	GENIC	homozygous	117540574
9	50726447	50726448	T	G	24	GENIC	homozygous	117540576
9	50729602	50729603	T	G	28	GENIC	homozygous	117540578
9	50730490	50730491	G	A	19	GENIC	homozygous	117540580
9	50738480	50738481	G	T	1	GENIC	homozygous	117540582
9	50738482	50738483	A	T	1	GENIC	homozygous	117540584
9	50738573	50738573		T	7	GENIC	possibly homozygous	128710274
9	50728214	50728215	C		33	GENIC	homozygous	128710270
9	50732671	50732672	A		27	GENIC	homozygous	128710271
9	50732903	50732904	T		15	GENIC	possibly homozygous	128710272
9	50735756	50735756		T	27	GENIC	heterozygous	128710273
9	50740428	50740429	A	C	29	GENIC	homozygous	117540586
9	50740504	50740505	C	T	32	GENIC	homozygous	117540588
9	50743194	50743195	G		21	GENIC	homozygous	128710275
9	50743613	50743613		TC	25	GENIC	homozygous	128710276
9	50744647	50744648	G	A	25	GENIC	homozygous	117540596
9	50740521	50740522	C	T	31	GENIC	homozygous	117540590
9	50740738	50740739	G	C	27	GENIC	homozygous	117540592
9	50741935	50741936	G	A	16	GENIC	homozygous	117335032
9	50743915	50743916	A	G	27	GENIC	homozygous	117540594