chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	79006071	79006072	A	T	53	GENIC	homozygous	143238665
5	79006987	79007008	TTTGACCTCTCAATGCACAAG		43	GENIC	homozygous	137319110
5	79007035	79007036	A	G	48	GENIC	homozygous	137519325
5	79007705	79007706	A	T	48	GENIC	homozygous	137519326
5	79008551	79008552	G	T	48	GENIC	homozygous	143238666
5	79008645	79008646	T	C	51	GENIC	homozygous	137519327
5	79008915	79008916	G	A	55	GENIC	homozygous	143238667
5	79011513	79011514	C		49	GENIC	homozygous	143182744
5	79011753	79011754	C	T	44	GENIC	homozygous	143238668
5	79011867	79011868	A	G	42	GENIC	homozygous	137519329
5	79014083	79014084	A	G	71	GENIC	homozygous	137519330
5	79015583	79015584	A	C	57	GENIC	homozygous	137519333
5	79015727	79015728	G	A	46	GENIC	possibly homozygous	137519334
5	79015766	79015767	G	A	47	GENIC	possibly homozygous	143238669
5	79015805	79015806	T	C	55	GENIC	possibly homozygous	143238670
5	79016124	79016130	TTCTGC		47	GENIC	possibly homozygous	143182745