chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61365342	61365343	A	T	12	GENIC	heterozygous	46690407
18	61365591	61365592	G	T	11	GENIC	possibly homozygous	46483563
18	61366058	61366059	T	C	10	GENIC	homozygous	46483568
18	61366089	61366090	C	G	15	GENIC	homozygous	46483569
18	61366283	61366284	G	A	9	GENIC	possibly homozygous	46483571
18	61366536	61366537	G	A	2	GENIC	homozygous	46483572
18	61367207	61367208	A	G	8	GENIC	homozygous	46483579
18	61367288	61367289	A	AC	12	GENIC	homozygous	46483580
18	61367351	61367352	T	A	20	GENIC	possibly homozygous	46483581
18	61367374	61367375	G	GTT	6	GENIC	heterozygous	46690408
18	61367374	61367375	G	GT	6	GENIC	heterozygous	46829687
18	61367467	61367468	A	G	15	GENIC	homozygous	46483583
18	61367570	61367571	G	T	19	GENIC	homozygous	46483584
18	61368285	61368286	G	C	10	GENIC	homozygous	46483585
18	61368317	61368318	T	G	10	GENIC	homozygous	46690409
18	61368365	61368366	G	T	19	GENIC	homozygous	46690410
18	61368515	61368516	T	C	13	GENIC	homozygous	46483586
18	61368576	61368577	T	C	24	GENIC	possibly homozygous	46483587
18	61368965	61368966	G	C	14	GENIC	homozygous	46483588