chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	56316429	56316430	G	C	41	GENIC	homozygous	109738376
19	56319857	56319858	G	A	54	GENIC	homozygous	109738380
19	56320468	56320469	A	G	46	GENIC	homozygous	109738382
19	56323710	56323711	C	T	65	GENIC	homozygous	109738384
19	56323790	56323791	C	T	40	GENIC	homozygous	109738386
19	56324840	56324841	T	C	58	GENIC	homozygous	109738388
19	56327463	56327464	T	C	43	GENIC	homozygous	109738390
19	56329037	56329038	A	G	48	GENIC	homozygous	109738392
19	56329567	56329568	T	C	33	GENIC	homozygous	119633753
19	56330031	56330032	G	A	52	GENIC	homozygous	109738394
19	56331021	56331022	C	A	46	GENIC	homozygous	109738396
19	56331700	56331701	A	T	62	GENIC	homozygous	109738398
19	56331834	56331835	A	G	58	GENIC	homozygous	109738400
19	56331903	56331904	G	A	57	GENIC	homozygous	109738402
19	56332006	56332007	A	G	53	GENIC	homozygous	109738404
19	56332572	56332573	G	A	55	GENIC	homozygous	109738406
19	56332602	56332603	G	T	45	GENIC	homozygous	109738408
19	56333272	56333273	C	T	54	GENIC	homozygous	109738410
19	56333651	56333652	A	T	49	GENIC	homozygous	109738412
19	56333857	56333858	C	T	47	GENIC	homozygous	109738414
19	56317349	56317349		A	52	GENIC	homozygous	129623386
19	56328067	56328067		A	12	GENIC	possibly homozygous	129623387
19	56329673	56329678	CCTGC		44	GENIC	homozygous	129623388
19	56331015	56331015		CTG	45	GENIC	homozygous	129623389
19	56331018	56331021	CCC		46	GENIC	homozygous	129623390
19	56331038	56331038		TC	45	GENIC	homozygous	129623391
19	56334558	56334559	A	G	46	GENIC	homozygous	109738416
19	56334811	56334811		AAC	22	GENIC	homozygous	133332716
19	56335185	56335196	CAGAGGAAGTC		6	GENIC	homozygous	129623392
19	56335440	56335441	C	T	37	GENIC	homozygous	109738418
19	56335441	56335442	G	A	35	GENIC	homozygous	109738420
19	56335443	56335444	A	C	35	GENIC	homozygous	109738422