chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	49185069	49185070	C	T	27	GENIC	homozygous	52971489
8	49185172	49185173	G	A	37	GENIC	homozygous	52971490
8	49185218	49185219	C	T	47	GENIC	homozygous	52971491
8	49185699	49185700	G	A	54	GENIC	homozygous	52971492
8	49186642	49186643	A	G	51	GENIC	possibly homozygous	52971493
8	49187126	49187127	C	T	40	GENIC	possibly homozygous	52971494
8	49187188	49187189	T	C	43	GENIC	homozygous	52971495
8	49187268	49187269	A	G	47	GENIC	possibly homozygous	52971496
8	49187461	49187462	C	-	46	GENIC	heterozygous	52971497
8	49187479	49187480	G	GA	50	GENIC	heterozygous	52971498
8	49187498	49187499	T	C	38	GENIC	homozygous	52971499