chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	138320516	138320517	G	A	51	GENIC	homozygous	114027309
5	138321353	138321354	G	T	63	GENIC	homozygous	114027310
5	138322125	138322126	T	A	67	GENIC	possibly homozygous	114027311
5	138322247	138322248	G	T	67	GENIC	homozygous	114027312
5	138324018	138324019	G	A	53	GENIC	homozygous	114027313
5	138324242	138324242		GAGAAAATTCCAGTCAAGACACAATCTTTCTCAAAAGCTGTAACGAGGAGCAGGGAGGGCTGCTGA	45	GENIC	homozygous	128244968
5	138324579	138324580	T	C	60	GENIC	homozygous	114027314
5	138325360	138325361	A		64	GENIC	homozygous	128244969
5	138325636	138325637	G	A	63	GENIC	homozygous	114027315
5	138326765	138326766	C	G	39	GENIC	heterozygous	132472756
5	138326808	138326809	A	T	38	GENIC	possibly homozygous	114027316
5	138328722	138328723	T	C	71	GENIC	homozygous	114027317
5	138328843	138328844	C	T	62	GENIC	homozygous	114027318
5	138329561	138329562	A		33	GENIC	possibly homozygous	128244970
5	138329576	138329579	AAG		36	GENIC	possibly homozygous	128244971
5	138329590	138329591	A	G	37	GENIC	possibly homozygous	128301098
5	138329961	138329962	T	C	48	GENIC	homozygous	114027319
5	138331513	138331514	A		60	GENIC	homozygous	128244972
5	138331827	138331827		TAAG	60	GENIC	homozygous	128244973
5	138332781	138332782	T	G	32	GENIC	homozygous	114027320
5	138332821	138332822	G	A	21	GENIC	homozygous	114027321
5	138332822	138332823	C	T	21	GENIC	homozygous	114027322
5	138332896	138332901	AGTTC		9	GENIC	homozygous	128244974
5	138333011	138333012	G	A	38	GENIC	homozygous	114027323
5	138333145	138333146	A	C	50	GENIC	homozygous	114027324
5	138334253	138334254	A		41	GENIC	homozygous	128244975
5	138336182	138336183	G	T	52	GENIC	homozygous	114027325