chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	4937996	4937997	T	C	30	GENIC	heterozygous	143717297
20	4940458	4940459	T	C	41	GENIC	homozygous	143717302
20	4940818	4940819	G	C	51	GENIC	homozygous	130034837
20	4938784	4938785	G	A	65	GENIC	homozygous	130034835
20	4940389	4940390	C	A	44	GENIC	homozygous	130034836
20	4941029	4941030	G	C	29	GENIC	homozygous	130034838
20	4942107	4942108	A	G	39	GENIC	homozygous	130034841
20	4942996	4942997	C	A	51	GENIC	homozygous	142725214
20	4943050	4943051	G	A	52	GENIC	homozygous	140511555
20	4943207	4943208	T	C	43	GENIC	homozygous	130034844
20	4943357	4943358	A	G	25	GENIC	homozygous	142725215
20	4943390	4943391	C	G	24	GENIC	homozygous	130034845
20	4943592	4943593	A	G	47	GENIC	homozygous	130034848
20	4943675	4943676	A	G	63	GENIC	homozygous	130034849
20	4942556	4942557	G	A	48	GENIC	homozygous	148798701
20	4943277	4943278	G	A	47	GENIC	homozygous	148798702
20	4943417	4943418	A	G	19	GENIC	homozygous	148798703
20	4943643	4943644	C	T	54	GENIC	homozygous	148798704
20	4943835	4943836	T	C	33	GENIC	homozygous	130034850
20	4944191	4944192	T	C	47	GENIC	homozygous	130034856
20	4945050	4945051	A	G	45	GENIC	homozygous	148798705
20	4945156	4945157	G	A	53	GENIC	homozygous	148798706
20	4945305	4945306	G	A	52	GENIC	homozygous	148798707
20	4944003	4944003		GC	39	GENIC	homozygous	148796292
20	4940921	4940921		CCATGCCTGTCAGGAGAGCACACAGACAGCG	32	GENIC	possibly homozygous	129980000
20	4943156	4943156		AG	42	GENIC	homozygous	147204844
20	4945604	4945605	T	C	57	GENIC	homozygous	130034861
20	4945778	4945779	G	T	43	GENIC	homozygous	148798708