chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	9287289	9287290	C	A	27	GENIC	homozygous	60622575
1	9287606	9287607	A	C	24	GENIC	homozygous	60622582
1	9289265	9289266	C	T	23	GENIC	homozygous	61370997
1	9289370	9289371	A	C	21	GENIC	homozygous	60622594
1	9289778	9289779	T	C	15	GENIC	homozygous	60622596
1	9289861	9289862	G	GTA	38	GENIC	homozygous	61370999
1	9289917	9289918	G	GTGTTGT	21	GENIC	homozygous	60622597
1	9290083	9290087	TCTT	----	22	GENIC	homozygous	61371001
1	9290705	9290706	T	C	38	GENIC	homozygous	60622598
1	9290779	9290780	G	A	25	GENIC	homozygous	61371003
1	9290930	9290931	G	A	25	GENIC	homozygous	61371005
1	9291226	9291227	A	G	37	GENIC	homozygous	61371007
1	9292554	9292555	T	A	19	GENIC	homozygous	60622601
1	9292564	9292565	G	T	23	GENIC	homozygous	60622602
1	9293382	9293383	T	C	34	GENIC	homozygous	61371009
1	9293444	9293445	G	T	27	GENIC	homozygous	61371010
1	9293879	9293880	G	A	23	GENIC	homozygous	61371012
1	9293905	9293906	T	C	33	GENIC	homozygous	60622605
1	9295208	9295209	G	A	31	GENIC	homozygous	61371014
1	9295318	9295319	C	T	25	GENIC	homozygous	61371016
1	9295532	9295533	C	A	34	GENIC	homozygous	61371018
1	9295986	9295987	G	-	29	GENIC	homozygous	61371020
1	9296698	9296699	A	C	21	GENIC	homozygous	61371022
1	9297841	9297842	T	C	32	GENIC	homozygous	61371024
1	9298015	9298016	T	C	13	GENIC	homozygous	61371026
1	9298023	9298024	C	CA	13	GENIC	homozygous	61371028
1	9298092	9298093	T	C	21	GENIC	homozygous	60622609
1	9298322	9298323	G	T	37	GENIC	homozygous	61371030
1	9298475	9298476	T	G	35	GENIC	homozygous	60622610
1	9299478	9299479	T	C	34	GENIC	homozygous	61371032
1	9299912	9299913	A	G	24	GENIC	homozygous	60622611
1	9300054	9300058	CAAA	----	37	GENIC	homozygous	61371034
1	9300132	9300133	G	GT	19	GENIC	homozygous	60622612
1	9300725	9300726	T	C	30	GENIC	homozygous	60622615
1	9301206	9301207	T	C	30	GENIC	homozygous	60622616
1	9301371	9301372	A	G	27	GENIC	homozygous	60622617
1	9301655	9301656	C	T	29	GENIC	homozygous	61371036
1	9301736	9301737	G	-	32	GENIC	possibly homozygous	60622619