chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	55669790	55669791	G	T	44	GENIC	homozygous	109942885
19	55670366	55670367	A	G	9	GENIC	homozygous	119720101
19	55671182	55671183	G	A	36	GENIC	possibly homozygous	109978509
19	55671932	55671933	G	A	59	GENIC	homozygous	109978511
19	55671945	55671946	G	A	50	GENIC	possibly homozygous	109978513
19	55672368	55672369	A	T	72	GENIC	homozygous	109942887
19	55672391	55672392	G	A	71	GENIC	homozygous	109978515
19	55672797	55672798	A	G	36	GENIC	homozygous	109942889
19	55673045	55673046	C	G	39	GENIC	homozygous	109978517
19	55674006	55674007	T	A	33	GENIC	homozygous	109978520
19	55674016	55674017	T	C	35	GENIC	homozygous	109978522
19	55674074	55674075	T	C	53	GENIC	homozygous	109942893
19	55674418	55674419	T	C	50	GENIC	homozygous	109942895
19	55674971	55674972	C	A	21	GENIC	homozygous	109997668
19	55675966	55675967	T	C	40	GENIC	homozygous	109978524
19	55676988	55676989	C	G	51	GENIC	homozygous	109942899
19	55678290	55678291	T	C	57	GENIC	homozygous	109942903
19	55678998	55678999	T	C	62	GENIC	homozygous	109942905
19	55679058	55679059	C	T	49	GENIC	homozygous	109942907
19	55679177	55679178	T	C	42	GENIC	homozygous	109737032
19	55680226	55680227	C	T	43	GENIC	possibly homozygous	109978526
19	55680372	55680373	T	C	42	GENIC	possibly homozygous	109978528
19	55680548	55680549	G	A	37	GENIC	homozygous	109978530
19	55681734	55681735	C	T	41	GENIC	homozygous	109978532
19	55684125	55684126	A	G	29	GENIC	homozygous	109789032