chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	66707649	66707650	T	G	41	GENIC	homozygous	46191833
19	66708662	66708663	A	AAGGGCAG	3	GENIC	homozygous	46191834
19	66708769	66708770	T	C	37	GENIC	homozygous	46191835
19	66708851	66708852	C	T	47	GENIC	homozygous	46191836
19	66709299	66709303	TCAA	----	31	GENIC	homozygous	46191837
19	66709316	66709317	T	C	49	GENIC	homozygous	46191838
19	66709358	66709359	T	C	56	GENIC	homozygous	46191839
19	66710563	66710564	C	T	35	GENIC	homozygous	46191840
19	66710763	66710764	A	G	48	GENIC	possibly homozygous	46191841
19	66711716	66711717	A	G	47	GENIC	possibly homozygous	46191842
19	66711984	66711985	A	T	45	GENIC	homozygous	46191843
19	66712151	66712152	A	G	39	GENIC	homozygous	46191844
19	66712457	66712458	C	T	51	GENIC	possibly homozygous	46191845
19	66712552	66712553	C	T	45	GENIC	homozygous	46191846
19	66713433	66713434	C	T	28	GENIC	homozygous	46191847
19	66713613	66713618	GGGTC	-----	2	GENIC	heterozygous	46191848
19	66713639	66713640	C	T	19	GENIC	possibly homozygous	46191849
19	66714030	66714031	A	G	43	GENIC	heterozygous	46191850
19	66714035	66714036	C	A	41	GENIC	heterozygous	46191851
19	66714053	66714054	G	A	37	GENIC	heterozygous	46191852
19	66714982	66714983	C	G	35	GENIC	homozygous	46191853