chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	50127272	50127273	A	G	51	GENIC	homozygous	46153458
19	50127488	50127489	C	T	20	GENIC	homozygous	46153459
19	50127613	50127621	AAAAAAAC	--------	18	GENIC	homozygous	46153460
19	50128059	50128060	T	C	39	GENIC	homozygous	46153461
19	50128612	50128613	T	C	41	GENIC	possibly homozygous	46153462
19	50128621	50128622	A	AAAAC	33	GENIC	homozygous	46153463
19	50129514	50129515	T	A	24	GENIC	heterozygous	46153465
19	50129888	50129889	A	ACACCC	23	GENIC	homozygous	46153466
19	50131011	50131012	A	G	29	GENIC	possibly homozygous	46153467
19	50131044	50131045	C	CA	26	GENIC	homozygous	46153468
19	50131158	50131159	A	G	40	GENIC	homozygous	46153469
19	50131335	50131336	T	C	20	GENIC	possibly homozygous	46153470
19	50131339	50131340	T	C	20	GENIC	possibly homozygous	46153471
19	50131346	50131347	T	C	19	GENIC	heterozygous	46153472
19	50131359	50131360	C	T	21	GENIC	heterozygous	46153473
19	50131364	50131365	T	TC	17	GENIC	possibly homozygous	46153474