chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	89330095	89330096	A	C	20	GENIC	homozygous	114571572
13	89333632	89333633	G	A	24	GENIC	homozygous	114571574
13	89336314	89336315	G	A	20	GENIC	homozygous	114571578
13	89336450	89336451	A	G	17	GENIC	homozygous	114571580
13	89336529	89336530	G	A	24	GENIC	homozygous	114571582
13	89336972	89336973	C	A	25	GENIC	possibly homozygous	114571584
13	89337796	89337797	T	C	17	GENIC	homozygous	114571586
13	89338362	89338363	T	G	25	GENIC	homozygous	114571588
13	89338901	89338902	G	A	30	GENIC	homozygous	114571590
13	89339270	89339271	C	G	33	GENIC	possibly homozygous	114571592
13	89340405	89340406	A	G	29	GENIC	homozygous	114571596
13	89340606	89340607	C	T	27	GENIC	homozygous	114571598
13	89341388	89341389	C	T	31	GENIC	homozygous	114571600
13	89341415	89341416	G	A	27	GENIC	homozygous	114571601
13	89341822	89341823	C	T	36	GENIC	homozygous	114571603
13	89341958	89341959	A	G	36	GENIC	possibly homozygous	114571605
13	89342077	89342078	T	C	24	GENIC	homozygous	114571607
13	89342464	89342465	T	C	31	GENIC	homozygous	114571609
13	89342628	89342629	G	A	24	GENIC	homozygous	114571611
13	89343113	89343114	G	A	32	GENIC	homozygous	114571613
13	89343264	89343265	G	A	25	GENIC	homozygous	114571615
13	89343495	89343496	T	C	17	GENIC	homozygous	114571617
13	89343496	89343497	G	A	17	GENIC	homozygous	114571619
13	89343543	89343544	T	G	15	GENIC	homozygous	114571621