chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50094075	50094076	A	C	25	GENIC	homozygous	118450533
13	50094089	50094090	C	T	25	GENIC	homozygous	118450534
13	50094109	50094110	G	A	34	GENIC	homozygous	118498269
13	50096116	50096117	T	C	57	GENIC	heterozygous	118498270
13	50096143	50096144	T	C	37	GENIC	heterozygous	118498271
13	50096301	50096302	T	C	34	GENIC	heterozygous	118498272
13	50096999	50097000	T	C	24	GENIC	heterozygous	115137027
13	50097001	50097002	T	C	24	GENIC	heterozygous	115137029
13	50098604	50098605	C	T	53	GENIC	homozygous	114670632
13	50097583	50097584	C	A	41	GENIC	homozygous	114670626
13	50097742	50097743	C	T	54	GENIC	homozygous	114670628
13	50098230	50098231	G	T	42	GENIC	homozygous	114339409
13	50108650	50108651	C	T	66	GENIC	homozygous	114339419
13	50128754	50128755	G	A	29	GENIC	heterozygous	118498273
13	50128758	50128759	G	A	21	GENIC	heterozygous	118498274
13	50131193	50131194	T	C	54	GENIC	homozygous	114339471
13	50131715	50131716	G	T	44	GENIC	homozygous	114339473
13	50132488	50132489	G	T	46	GENIC	homozygous	114549917
13	50136457	50136458	G	A	63	GENIC	homozygous	114339475
13	50139874	50139875	C	T	29	GENIC	heterozygous	118498275
13	50147647	50147648	C	A	52	GENIC	homozygous	114339479
13	50148674	50148675	T	C	52	GENIC	homozygous	114339481
13	50127226	50127227	C	T	65	GENIC	possibly homozygous	114762024
13	50148797	50148798	C	T	64	GENIC	homozygous	114339483
13	50150078	50150079	A	G	52	GENIC	homozygous	114339485
13	50150431	50150432	T	C	69	GENIC	homozygous	114762026
13	50151242	50151243	A	G	46	GENIC	homozygous	114339487
13	50152886	50152887	G	A	63	GENIC	possibly homozygous	114339489