chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	134959567	134959568	A	G	36	GENIC	homozygous	114993403
6	134965939	134965940	T	C	33	GENIC	homozygous	114993410
6	134970311	134970312	C	T	30	GENIC	homozygous	115300521
6	134971543	134971544	G	C	26	GENIC	homozygous	114993413
6	134975789	134975790	T	C	45	GENIC	possibly homozygous	114993418
6	134978259	134978260	G	C	26	GENIC	possibly homozygous	115300523
6	134978872	134978873	C	T	21	GENIC	possibly homozygous	115300525
6	134981170	134981171	T	A	45	GENIC	homozygous	114993421
6	134981387	134981388	C	A	19	GENIC	possibly homozygous	114993422
6	134983170	134983171	C	T	34	GENIC	homozygous	115300527
6	134985046	134985047	G	A	26	GENIC	homozygous	115300529
6	134985780	134985781	C	T	40	GENIC	homozygous	115300531
6	134986921	134986922	T	C	43	GENIC	homozygous	114993427
6	134987140	134987141	C	T	42	GENIC	homozygous	115300533
6	134987361	134987362	A	G	29	GENIC	possibly homozygous	114993428
6	134987602	134987603	G	T	39	GENIC	homozygous	114993429
6	134988679	134988680	G	A	38	GENIC	homozygous	114993430
6	134990730	134990731	A	G	38	GENIC	possibly homozygous	115300535
6	134992294	134992295	G	C	37	GENIC	possibly homozygous	114993435
6	134996002	134996003	C	T	28	GENIC	homozygous	115300537
6	134999159	134999160	T	C	45	GENIC	homozygous	114993441
6	135000807	135000808	A	G	33	GENIC	homozygous	115300539
6	135001899	135001900	G	A	44	GENIC	homozygous	114993445
6	135004524	135004525	G	A	26	GENIC	homozygous	115300541
6	135074741	135074742	T	C	31	GENIC	homozygous	114993448