chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	144061259	144061260	C	G	43	GENIC	homozygous	137644978
5	144062422	144062423	T	C	59	GENIC	homozygous	137644979
5	144062811	144062812	A	G	58	GENIC	homozygous	137644980
5	144062831	144062832	A	G	65	GENIC	homozygous	137644981
5	144063025	144063026	G	A	52	GENIC	homozygous	137644982
5	144063213	144063214	C	T	56	GENIC	homozygous	137644983
5	144064134	144064135	G		24	GENIC	possibly homozygous	137347486
5	144065145	144065146	A	G	51	GENIC	homozygous	137644984
5	144065890	144065891	A	C	49	GENIC	homozygous	137644985
5	144066570	144066571	T	C	73	GENIC	homozygous	137644986
5	144066789	144066790	T		47	GENIC	homozygous	137347487
5	144067442	144067443	G	A	73	GENIC	homozygous	137644987
5	144067952	144067953	A	G	47	GENIC	possibly homozygous	137644988
5	144068145	144068146	A	T	57	GENIC	homozygous	137644989
5	144068571	144068572	A	G	66	GENIC	homozygous	137644990
5	144069052	144069053	A	G	73	GENIC	homozygous	137644991
5	144069585	144069586	G	T	73	GENIC	homozygous	137644992
5	144070117	144070117		TTAT	34	GENIC	homozygous	137347488
5	144071576	144071576		C	49	GENIC	homozygous	137347489
5	144072427	144072428	G	T	64	GENIC	homozygous	137644993
5	144074249	144074250	A	G	50	GENIC	homozygous	137644994
5	144075149	144075150	C	T	61	GENIC	homozygous	137644995
5	144085881	144085882	A		57	GENIC	possibly homozygous	137347490
5	144089689	144089689		GCT	37	GENIC	possibly homozygous	137347491
5	144090001	144090002	T	G	39	GENIC	homozygous	137645000
5	144079347	144079348	A	T	54	GENIC	homozygous	137644996
5	144080360	144080361	G	A	54	GENIC	homozygous	137644997
5	144083372	144083373	G	A	24	GENIC	homozygous	137644998
5	144089679	144089680	T	A	36	GENIC	possibly homozygous	137644999