chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	60909552	60909553	C	A	129	GENIC	heterozygous	118455072
13	60910601	60910602	A	G	66	GENIC	heterozygous	118543917
13	60910659	60910660	G	A	53	GENIC	heterozygous	118543918
13	60912157	60912158	T	C	15	GENIC	heterozygous	118543919
13	60912653	60912654	C	A	161	GENIC	heterozygous	118543920
13	60912788	60912789	T	C	85	GENIC	heterozygous	118543921
13	60913265	60913266	G	A	44	GENIC	heterozygous	118523539
13	60916056	60916057	G	T	47	GENIC	heterozygous	118523542
13	60916088	60916089	G	A	30	GENIC	heterozygous	118455074
13	60916103	60916104	A	G	24	GENIC	possibly homozygous	118455075
13	60917253	60917254	T	A	5	GENIC	homozygous	118543922
13	60918646	60918647	A	G	34	GENIC	homozygous	114366213
13	60920020	60920021	C	G	52	GENIC	homozygous	114366216
13	60920776	60920777	G	A	42	GENIC	homozygous	114366219
13	60922687	60922688	C	A	39	GENIC	homozygous	114678523
13	60922853	60922854	A	G	30	GENIC	homozygous	114625639
13	60923011	60923012	T	C	42	GENIC	homozygous	114625641
13	60923130	60923131	C	G	45	GENIC	homozygous	114625643
13	60923388	60923389	T	C	50	GENIC	homozygous	114625645
13	60923518	60923519	T	C	35	GENIC	heterozygous	118543923
13	60923564	60923565	C	T	50	GENIC	heterozygous	118543924
13	60923591	60923592	T	C	35	GENIC	possibly homozygous	118523543
13	60923595	60923596	T	C	35	GENIC	possibly homozygous	118523544
13	60923607	60923608	C	T	37	GENIC	possibly homozygous	118523545
13	60923912	60923913	T	C	27	GENIC	possibly homozygous	114625647
13	60924032	60924033	C	T	41	GENIC	homozygous	114625649
13	60924035	60924036	G	A	41	GENIC	homozygous	114625651
13	60924374	60924375	C	T	13	GENIC	homozygous	114625653
13	60925013	60925014	T	C	16	GENIC	homozygous	118523546