chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	85689249	85689250	G	A	32	GENIC	homozygous	61455258
1	85690131	85690132	T	TCA	30	GENIC	possibly homozygous	61455259
1	85691839	85691840	T	C	16	GENIC	homozygous	61455261
1	85691873	85691874	C	T	16	GENIC	homozygous	62687352
1	85691886	85691887	T	C	19	GENIC	homozygous	61455262
1	85692429	85692430	C	CT	14	GENIC	heterozygous	62261785
1	85692429	85692430	C	CTTT	14	GENIC	heterozygous	62261786
1	85693317	85693318	A	G	9	GENIC	homozygous	61455265
1	85693389	85693390	T	C	12	GENIC	homozygous	61455266
1	85697652	85697653	C	CGTGTGT	15	GENIC	homozygous	62013292
1	85698117	85698118	G	A	17	GENIC	homozygous	62687353
1	85698953	85698954	C	T	15	GENIC	homozygous	62687354
1	85699073	85699074	C	T	12	GENIC	homozygous	62687355
1	85699210	85699211	T	C	15	GENIC	homozygous	62687356
1	85699520	85699522	AC	--	4	GENIC	heterozygous	61297400
1	85699740	85699741	A	AACAC	19	GENIC	homozygous	62687357
1	85701095	85701101	TATCTA	------	22	GENIC	homozygous	62687358
1	85703386	85703387	C	A	23	GENIC	homozygous	62687359
1	85703413	85703414	T	C	16	GENIC	homozygous	62687360
1	85704323	85704324	A	G	1	GENIC	homozygous	62687361
1	85704414	85704415	T	TAA	2	GENIC	homozygous	62639660