chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	81683338	81683339	A	T	47	GENIC	homozygous	115077856
13	81685083	81685084	G	A	50	GENIC	homozygous	115077858
13	81688867	81688868	G	T	47	GENIC	homozygous	115077860
13	81688924	81688925	G	C	50	GENIC	homozygous	115077862
13	81689269	81689270	G	A	40	GENIC	homozygous	115077864
13	81689548	81689549	T	C	42	GENIC	homozygous	114409837
13	81689072	81689072		C	31	GENIC	homozygous	129078949
13	81690897	81690898	C	T	43	GENIC	homozygous	115077866
13	81691992	81691993	C	A	37	GENIC	possibly homozygous	115077868
13	81692832	81692833	C	T	35	GENIC	homozygous	115077870
13	81692930	81692931	T	A	43	GENIC	homozygous	114409852
13	81693381	81693382	C	T	43	GENIC	homozygous	114409854
13	81697041	81697042	G	A	59	GENIC	homozygous	115077872
13	81692764	81692776	GTGTGTGAGTGT		28	GENIC	homozygous	131504867