chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61365512	61365513	T	C	3	GENIC	homozygous	46483562
18	61365591	61365592	G	T	16	GENIC	homozygous	46483563
18	61366037	61366038	C	G	27	GENIC	possibly homozygous	46483567
18	61366058	61366059	T	C	22	GENIC	possibly homozygous	46483568
18	61366089	61366090	C	G	16	GENIC	possibly homozygous	46483569
18	61366218	61366219	T	G	21	GENIC	possibly homozygous	46483570
18	61366283	61366284	G	A	13	GENIC	possibly homozygous	46483571
18	61366536	61366537	G	A	9	GENIC	homozygous	46483572
18	61366558	61366559	G	A	2	GENIC	homozygous	46483573
18	61366569	61366570	G	T	2	GENIC	homozygous	46483574
18	61366628	61366641	ATTGGGCAATGTC	-------------	2	GENIC	homozygous	46483577
18	61367046	61367047	G	A	6	GENIC	homozygous	46483578
18	61367207	61367208	A	G	12	GENIC	homozygous	46483579
18	61367288	61367289	A	AC	11	GENIC	homozygous	46483580
18	61367351	61367352	T	A	11	GENIC	possibly homozygous	46483581
18	61367467	61367468	A	G	17	GENIC	homozygous	46483583
18	61367570	61367571	G	T	19	GENIC	homozygous	46483584
18	61368285	61368286	G	C	17	GENIC	possibly homozygous	46483585
18	61368515	61368516	T	C	16	GENIC	homozygous	46483586
18	61368576	61368577	T	C	19	GENIC	possibly homozygous	46483587
18	61368965	61368966	G	C	15	GENIC	homozygous	46483588