chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	47939862	47939863	G	C	40	GENIC	homozygous	114760424
13	47940056	47940057	G	A	22	GENIC	homozygous	114823699
13	47941790	47941791	A	G	47	GENIC	homozygous	114548493
13	47942595	47942596	C	T	27	GENIC	homozygous	114823701
13	47944260	47944261	T	C	41	GENIC	heterozygous	118497655
13	47946450	47946451	T	A	54	GENIC	homozygous	114823703
13	47947515	47947516	G	A	42	GENIC	homozygous	114548498
13	47948280	47948281	C	T	35	GENIC	homozygous	114823705
13	47949001	47949002	T	C	52	GENIC	homozygous	114548499
13	47949638	47949639	T	C	43	GENIC	homozygous	114548500
13	47950094	47950095	T	C	49	GENIC	possibly homozygous	118497656
13	47950517	47950518	A	C	46	GENIC	homozygous	114548501
13	47951030	47951031	A	G	45	GENIC	homozygous	114548502
13	47951456	47951457	C	T	34	GENIC	homozygous	114823707
13	47951595	47951596	C	T	35	GENIC	homozygous	114548503
13	47952441	47952442	G	A	31	GENIC	homozygous	114615328
13	47953547	47953548	A	G	43	GENIC	homozygous	114548504
13	47953725	47953726	A	G	34	GENIC	homozygous	114548505
13	47954193	47954194	C	G	30	GENIC	homozygous	114548506
13	47954990	47954991	A	G	16	GENIC	possibly homozygous	114669036
13	47955127	47955128	A	G	37	GENIC	homozygous	114823709
13	47957559	47957560	A	G	51	GENIC	homozygous	114548513
13	47957710	47957711	T	C	35	GENIC	homozygous	114548514