chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	89726013	89726014	G	A	44	GENIC	homozygous	114572224
13	89726240	89726241	T	C	39	GENIC	homozygous	114572226
13	89726258	89726259	G	A	37	GENIC	homozygous	114572228
13	89726601	89726602	C	T	57	GENIC	homozygous	114572230
13	89728283	89728284	G	A	46	GENIC	homozygous	114572232
13	89728524	89728525	A	G	60	GENIC	homozygous	114572234
13	89729103	89729104	G	A	63	GENIC	homozygous	114572236
13	89730202	89730203	C	T	44	GENIC	homozygous	114572238
13	89728960	89728964	TGCA		38	GENIC	homozygous	131133829
13	89728971	89728971		GTGCAT	38	GENIC	homozygous	131133830
13	89730996	89730997	G	T	25	GENIC	homozygous	118503898
13	89732433	89732433		CTCCCTCTCCCT	29	GENIC	homozygous	131133831
13	89738441	89738442	C	G	70	GENIC	homozygous	114572240
13	89738768	89738769	G	T	58	GENIC	homozygous	114572242
13	89739724	89739725	G	T	51	GENIC	homozygous	118503903
13	89740874	89740875	T	C	68	GENIC	homozygous	114572244
13	89740981	89740982	T	G	51	GENIC	homozygous	114572246
13	89742658	89742659	A	G	69	GENIC	homozygous	114572248
13	89734727	89734728	T		31	GENIC	homozygous	131921134