chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	89602165	89602166	A	G	22	INTERGENIC	homozygous	49856268
13	89602693	89602694	A	G	21	INTERGENIC	homozygous	49856269
13	89602711	89602712	A	C	27	INTERGENIC	homozygous	49856270
13	89602869	89602870	A	C	25	INTERGENIC	homozygous	49856271
13	89603181	89603182	G	A	21	INTERGENIC	homozygous	49856272
13	89603686	89603687	A	G	24	INTERGENIC	homozygous	49856273
13	89603688	89603689	G	A	24	INTERGENIC	homozygous	49856274
13	89603712	89603713	G	A	28	INTERGENIC	homozygous	49856275
13	89603715	89603716	T	G	27	INTERGENIC	homozygous	49856276
13	89603716	89603717	A	C	27	INTERGENIC	homozygous	49856277
13	89603850	89603851	C	T	27	INTERGENIC	homozygous	49856278
13	89603929	89603930	A	-	20	INTERGENIC	homozygous	49856279
13	89604023	89604024	C	T	11	INTERGENIC	homozygous	49856280
13	89604052	89604053	C	G	10	INTERGENIC	homozygous	49856281
13	89604560	89604561	C	T	9	INTERGENIC	homozygous	49856290
13	89604679	89604680	A	G	20	INTERGENIC	homozygous	49856293
13	89605445	89605446	T	TCA	26	INTERGENIC	homozygous	49856294
13	89605625	89605626	G	A	19	INTERGENIC	homozygous	49856295
13	89605745	89605746	T	C	16	INTERGENIC	homozygous	49856296
13	89605831	89605832	G	A	12	INTERGENIC	possibly homozygous	49856297
13	89606051	89606052	G	C	27	INTERGENIC	homozygous	49856299