chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	130094701	130094704	AGG	---	3	GENIC	homozygous	57672194
3	130095151	130095152	A	G	6	GENIC	homozygous	57672196
3	130095935	130095936	C	T	2	GENIC	homozygous	60270296
3	130096087	130096088	G	A	3	GENIC	homozygous	60270297
3	130096959	130096960	C	T	6	GENIC	homozygous	60270298
3	130097050	130097051	T	C	11	GENIC	homozygous	57672198
3	130097218	130097219	C	T	8	GENIC	homozygous	60270299
3	130098261	130098262	C	CTACTGCGCTCTGGGCCCCGGGG	3	GENIC	homozygous	58695777
3	130098320	130098321	A	C	5	GENIC	homozygous	57672200
3	130098969	130098979	GTGTGTGTGT	----------	3	GENIC	homozygous	60284854
3	130099519	130099520	A	G	6	GENIC	homozygous	60023817
3	130100880	130100881	G	A	15	GENIC	homozygous	57672206
3	130100996	130100997	C	-	5	GENIC	homozygous	60023818
3	130101048	130101049	T	C	6	GENIC	homozygous	60023819
3	130101240	130101241	C	T	4	GENIC	homozygous	60023820
3	130101468	130101469	A	ATTCTGACCT	8	GENIC	homozygous	58534907
3	130101707	130101708	G	C	7	GENIC	homozygous	60023821
3	130102013	130102014	G	C	6	GENIC	homozygous	60023822
3	130102387	130102388	C	T	5	GENIC	homozygous	60023823
3	130102489	130102490	T	C	7	GENIC	homozygous	60023824
3	130103536	130103537	G	A	7	GENIC	homozygous	60023825
3	130103705	130103706	T	C	6	GENIC	homozygous	58534912
3	130105336	130105337	C	G	5	GENIC	homozygous	57672219
3	130105343	130105344	C	T	5	GENIC	homozygous	57672221
3	130105465	130105466	G	-	2	GENIC	homozygous	60270300
3	130105628	130105629	G	A	5	GENIC	homozygous	58534915
3	130106730	130106731	T	C	9	GENIC	homozygous	60270301