chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	54972137	54972138	A	C	30	GENIC	homozygous	46166474
19	54972980	54972981	T	TG	30	GENIC	homozygous	46166475
19	54974314	54974315	T	TTGTGTGTGTG	6	GENIC	homozygous	46166477
19	54974525	54974526	A	G	34	GENIC	possibly homozygous	46263644
19	54975009	54975010	T	A	43	GENIC	homozygous	46263645
19	54975079	54975080	T	A	19	GENIC	homozygous	46263646
19	54975089	54975090	G	T	13	GENIC	homozygous	46263647
19	54975351	54975352	T	C	22	GENIC	homozygous	46263648
19	54975389	54975390	T	C	29	GENIC	homozygous	46166485
19	54975429	54975430	A	T	37	GENIC	possibly homozygous	46166487
19	54975444	54975445	T	C	35	GENIC	possibly homozygous	46166488
19	54975567	54975568	A	T	55	GENIC	homozygous	46166489
19	54975733	54975734	G	C	35	GENIC	homozygous	46263649
19	54976564	54976565	G	GAATT	44	GENIC	homozygous	46263650
19	54976783	54976784	G	A	33	GENIC	homozygous	46166491
19	54976928	54976929	T	C	43	GENIC	homozygous	46166492
19	54977357	54977358	T	TTC	32	GENIC	homozygous	46166494
19	54978086	54978092	GAAGTG	------	16	GENIC	homozygous	46166496
19	54979381	54979382	C	T	39	GENIC	homozygous	46166497
19	54979723	54979724	C	T	31	GENIC	homozygous	46166498
19	54980778	54980779	C	T	30	GENIC	homozygous	46166499
19	54980799	54980800	T	C	30	GENIC	homozygous	46166500
19	54981068	54981069	A	G	28	GENIC	possibly homozygous	46166502
19	54981247	54981248	C	A	33	GENIC	homozygous	46166503
19	54981345	54981346	C	T	34	GENIC	homozygous	46166504
19	54981471	54981472	C	T	44	GENIC	possibly homozygous	46263651
19	54982285	54982286	T	G	25	GENIC	heterozygous	46274794
19	54982463	54982464	A	AAT	34	GENIC	homozygous	46263652
19	54982499	54982500	G	A	48	GENIC	homozygous	46263653
19	54982504	54982505	T	C	46	GENIC	homozygous	46166506