chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	53650208	53650209	C	T	28	GENIC	homozygous	109731850
19	53657556	53657557	A	G	40	GENIC	homozygous	109731852
19	53657691	53657692	A	G	28	GENIC	homozygous	109731854
19	53658115	53658116	A	C	50	GENIC	homozygous	109731856
19	53662885	53662886	T	C	26	GENIC	homozygous	109731858
19	53663525	53663526	T	C	37	GENIC	homozygous	109731860
19	53667288	53667289	T	C	24	GENIC	homozygous	109731862
19	53668422	53668423	A	C	7	GENIC	possibly homozygous	109997628
19	53676376	53676377	G	C	18	GENIC	homozygous	109731865
19	53678388	53678389	C	T	34	GENIC	homozygous	109731867
19	53680481	53680482	C	A	26	GENIC	homozygous	109731869
19	53681489	53681490	G	A	29	GENIC	homozygous	109731871
19	53682703	53682704	C	T	27	GENIC	homozygous	109731873
19	53685274	53685275	A	C	21	GENIC	homozygous	109825424
19	53687193	53687194	T	G	37	GENIC	homozygous	109731875