chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	144061259	144061260	C	G	23	GENIC	homozygous	137644978
5	144062422	144062423	T	C	23	GENIC	homozygous	137644979
5	144062751	144062752	A	C	25	GENIC	heterozygous	154259543
5	144062751	144062752	A	G	25	GENIC	homozygous	154259544
5	144062811	144062812	A	G	33	GENIC	homozygous	137644980
5	144062831	144062832	A	G	31	GENIC	homozygous	137644981
5	144064134	144064135	G		10	GENIC	homozygous	137347486
5	144065145	144065146	A	G	32	GENIC	homozygous	137644984
5	144065890	144065891	A	C	39	GENIC	homozygous	137644985
5	144066570	144066571	T	C	37	GENIC	homozygous	137644986
5	144066789	144066790	T		26	GENIC	homozygous	137347487
5	144067442	144067443	G	A	40	GENIC	homozygous	137644987
5	144068145	144068146	A	T	33	GENIC	homozygous	137644989
5	144068571	144068572	A	G	24	GENIC	homozygous	137644990
5	144069052	144069053	A	G	29	GENIC	homozygous	137644991
5	144069585	144069586	G	T	24	GENIC	homozygous	137644992
5	144070117	144070117		TTAT	23	GENIC	homozygous	137347488
5	144071576	144071576		C	16	GENIC	homozygous	137347489
5	144072433	144072438	TACAA		29	GENIC	homozygous	141690925
5	144074249	144074250	A	G	26	GENIC	homozygous	137644994
5	144078620	144078620		G	25	GENIC	homozygous	141690926
5	144079796	144079796		CGTTGTT	18	GENIC	homozygous	141690927
5	144080042	144080043	G	A	24	GENIC	homozygous	141766190
5	144077860	144077861	T	A	18	GENIC	homozygous	141766187
5	144078103	144078104	G	A	31	GENIC	homozygous	141766188
5	144079514	144079515	C	T	31	GENIC	homozygous	141766189
5	144080360	144080361	G	A	24	GENIC	homozygous	137644997
5	144082364	144082365	T	C	30	GENIC	homozygous	141766191
5	144084507	144084508	C	T	37	GENIC	homozygous	141766192
5	144084553	144084554	G	A	36	GENIC	homozygous	141766193
5	144085881	144085882	A		20	GENIC	possibly homozygous	137347490
5	144088118	144088119	T	C	28	GENIC	homozygous	141766194
5	144090058	144090059	G	A	23	GENIC	homozygous	141766195