chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56001804	56001805	C	T	48	GENIC	homozygous	110087532
19	56001909	56001910	C	G	54	GENIC	homozygous	110087534
19	56002837	56002838	G	A	69	GENIC	homozygous	110087536
19	56003262	56003263	G	A	65	GENIC	homozygous	110087538
19	56003271	56003272	A	G	67	GENIC	homozygous	110087540
19	56003316	56003317	T	C	63	GENIC	homozygous	109737558
19	56004290	56004291	A	C	53	GENIC	homozygous	110087542
19	56004884	56004885	A	G	67	GENIC	possibly homozygous	110087544
19	56005814	56005815	G	A	61	GENIC	homozygous	110087546
19	56006263	56006264	A	G	49	GENIC	homozygous	109737566
19	56006321	56006322	C		53	GENIC	homozygous	133511723
19	56003225	56003225		GGGCAGT	68	GENIC	possibly homozygous	133511721
19	56004317	56004317		C	49	GENIC	homozygous	133511722
19	56003255	56003256	T	C	65	GENIC	homozygous	133516666
19	56003856	56003857	T	G	46	GENIC	homozygous	133516667
19	56003920	56003921	G	T	58	GENIC	homozygous	133516668
19	56003863	56003864	T	C	48	GENIC	homozygous	109789087
19	56003905	56003906	T	C	57	GENIC	homozygous	109789089
19	56006698	56006699	A	G	47	GENIC	possibly homozygous	109737570
19	56007004	56007005	C	T	41	GENIC	homozygous	109737572
19	56008562	56008562		GACACTAGGGTCTGCGGAT	40	GENIC	homozygous	129623282
19	56009151	56009152	C	T	46	GENIC	homozygous	110087548