chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	9841368	9841369	A	T	15	GENIC	homozygous	51725255
9	9841373	9841374	G	A	14	GENIC	homozygous	51725257
9	9841398	9841399	A	C	10	GENIC	homozygous	51725259
9	9841399	9841400	T	C	10	GENIC	homozygous	51725261
9	9841420	9841421	C	T	11	GENIC	heterozygous	51725263
9	9841422	9841423	A	C	11	GENIC	homozygous	51725265
9	9841429	9841432	ATT	---	7	GENIC	heterozygous	51725267
9	9841439	9841440	A	-	6	GENIC	heterozygous	51725270
9	9841445	9841446	A	-	8	GENIC	heterozygous	51725272
9	9841447	9841448	C	-	8	GENIC	heterozygous	51725274
9	9841451	9841454	CAT	---	11	GENIC	heterozygous	51725276
9	9841499	9841502	CTC	---	24	GENIC	heterozygous	51725278
9	9841507	9841508	C	T	37	GENIC	heterozygous	51725280
9	9841546	9841547	T	C	34	GENIC	heterozygous	51725284
9	9846335	9846336	C	G	33	GENIC	homozygous	51725288
9	9849895	9849911	GGCACCTGTGTGGGGG	----------------	7	GENIC	homozygous	51725290
9	9850004	9850005	T	G	16	GENIC	heterozygous	51725292
9	9858944	9858945	G	-	11	GENIC	homozygous	51725300
9	9850381	9850382	G	-	5	GENIC	heterozygous	51725296
9	9858921	9858922	C	T	35	GENIC	homozygous	51725298
9	9858977	9858978	C	T	16	GENIC	homozygous	51725304
9	9859025	9859026	A	-	8	GENIC	homozygous	51725307
9	9859034	9859035	C	-	8	GENIC	homozygous	51725309
9	9859045	9859046	C	-	8	GENIC	homozygous	51725311
9	9859051	9859052	C	G	12	GENIC	possibly homozygous	51725313