chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
16	40992495	40992496	T	TGC	38	GENIC	heterozygous	47392478
16	40992498	40992500	GC	--	38	GENIC	possibly homozygous	47392480
16	40993416	40993417	G	GA	14	GENIC	homozygous	47392482
16	40994251	40994252	T	C	43	GENIC	homozygous	47392484
16	40996303	40996309	CACACA	------	15	GENIC	heterozygous	47392486
16	40996305	40996309	CACA	----	15	GENIC	heterozygous	47392488
16	40997021	40997022	A	AG	34	GENIC	homozygous	47392490
16	40997083	40997084	A	G	42	GENIC	heterozygous	47392492
16	40997083	40997084	A	AG	38	GENIC	heterozygous	47392494
16	40997413	40997415	AA	--	19	GENIC	homozygous	47392496
16	40997614	40997615	T	-	36	GENIC	homozygous	47392498
16	40999091	40999092	G	A	39	GENIC	homozygous	47392500
16	41000877	41000878	T	C	27	GENIC	heterozygous	47392502
16	41000889	41000890	T	C	29	GENIC	heterozygous	47392504
16	41001276	41001277	C	T	36	GENIC	homozygous	47392506
16	41002589	41002590	T	TC	18	GENIC	homozygous	47392508