chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	60909493	60909494	C	T	16	GENIC	possibly homozygous	118523533
13	60909592	60909593	G	A	85	GENIC	heterozygous	118523534
13	60912262	60912263	A	T	54	GENIC	heterozygous	118523535
13	60912392	60912393	C	A	86	GENIC	heterozygous	118523536
13	60912881	60912882	A	G	85	GENIC	heterozygous	118523537
13	60912886	60912887	A	G	87	GENIC	heterozygous	118523538
13	60913265	60913266	G	A	18	GENIC	heterozygous	118523539
13	60913580	60913581	G	A	56	GENIC	heterozygous	118523540
13	60915950	60915951	T	C	44	GENIC	heterozygous	118523541
13	60915958	60915959	C	T	50	GENIC	heterozygous	118499791
13	60916056	60916057	G	T	16	GENIC	heterozygous	118523542
13	60916088	60916089	G	A	13	GENIC	heterozygous	118455074
13	60916186	60916187	C	T	3	GENIC	homozygous	118455076
13	60916199	60916200	G	A	3	GENIC	homozygous	118455077
13	60918646	60918647	A	G	24	GENIC	homozygous	114366213
13	60920020	60920021	C	G	25	GENIC	homozygous	114366216
13	60920776	60920777	G	A	19	GENIC	homozygous	114366219
13	60922853	60922854	A	G	30	GENIC	possibly homozygous	114625639
13	60923011	60923012	T	C	15	GENIC	homozygous	114625641
13	60923130	60923131	C	G	12	GENIC	homozygous	114625643
13	60923388	60923389	T	C	21	GENIC	homozygous	114625645
13	60923591	60923592	T	C	8	GENIC	homozygous	118523543
13	60923595	60923596	T	C	9	GENIC	homozygous	118523544
13	60923607	60923608	C	T	9	GENIC	homozygous	118523545
13	60923912	60923913	T	C	22	GENIC	homozygous	114625647
13	60924032	60924033	C	T	24	GENIC	homozygous	114625649
13	60924035	60924036	G	A	24	GENIC	homozygous	114625651
13	60924374	60924375	C	T	13	GENIC	homozygous	114625653
13	60925013	60925014	T	C	19	GENIC	homozygous	118523546
13	60922687	60922688	C	A	27	GENIC	possibly homozygous	114678523