chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89485248	89485250	TT		17	GENIC	homozygous	131468992
10	89488017	89488018	G	A	39	GENIC	homozygous	116820155
10	89485318	89485319	A	T	11	GENIC	possibly homozygous	116950574
10	89487455	89487456	A	C	49	GENIC	homozygous	116950576
10	89485336	89485337	A	G	17	GENIC	homozygous	116820151
10	89487662	89487663	T	G	43	GENIC	possibly homozygous	116820153
10	89486477	89486478	G	A	32	GENIC	homozygous	116902655
10	89488278	89488279	G	A	38	GENIC	homozygous	116820157
10	89488471	89488472	C	T	42	GENIC	homozygous	116820159
10	89489238	89489239	T	C	44	GENIC	homozygous	116675621
10	89489955	89489956	A		31	GENIC	homozygous	131468993
10	89490480	89490481	T	G	43	GENIC	homozygous	116820163
10	89489809	89489810	A	G	56	GENIC	homozygous	118007575
10	89490757	89490758	T	C	26	GENIC	homozygous	123401618
10	89491133	89491138	GATTA		51	GENIC	homozygous	131468994
10	89491448	89491448		TC	33	GENIC	possibly homozygous	131468995
10	89492249	89492250	A	G	51	GENIC	homozygous	116675623
10	89492264	89492265	A	G	52	GENIC	homozygous	116675625
10	89493139	89493140	G	A	48	GENIC	homozygous	116820169
10	89493165	89493166	T	C	47	GENIC	homozygous	116675631