chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	46050213	46050214	A	C	48	GENIC	homozygous	130119604
20	46052040	46052040		TATC	30	GENIC	possibly homozygous	130001813
20	46058931	46058932	C	T	64	GENIC	homozygous	130119605
20	46059071	46059072	T	C	58	GENIC	homozygous	130119606
20	46059198	46059198		CTAA	39	GENIC	homozygous	130001814
20	46059498	46059499	G	A	45	GENIC	possibly homozygous	130119607
20	46061101	46061102	C	G	51	GENIC	homozygous	130119608
20	46061159	46061160	C	T	62	GENIC	homozygous	130119609
20	46061677	46061678	C		46	GENIC	possibly homozygous	130001816
20	46061679	46061680	C	T	46	GENIC	possibly homozygous	130119610
20	46061932	46061940	AATTTGCC		41	GENIC	possibly homozygous	130001817
20	46062126	46062127	G	A	44	GENIC	homozygous	130119611
20	46062568	46062569	T	G	48	GENIC	homozygous	130119612
20	46063512	46063513	A	G	45	GENIC	possibly homozygous	130119613
20	46063607	46063608	C	T	37	GENIC	homozygous	130119614
20	46063754	46063757	GTG		49	GENIC	homozygous	130001818
20	46063758	46063759	T	C	52	GENIC	homozygous	130119615
20	46066587	46066587		A	49	GENIC	possibly homozygous	130001819
20	46067043	46067044	C	G	50	GENIC	homozygous	130119616
20	46067935	46067936	C	T	60	GENIC	homozygous	130119617
20	46068517	46068518	T	C	65	GENIC	homozygous	130119618
20	46068550	46068551	A	G	48	GENIC	homozygous	130119619
20	46068611	46068612	C	T	41	GENIC	homozygous	130119620
20	46068710	46068711	T	C	29	GENIC	homozygous	130119621
20	46069766	46069767	T	C	41	GENIC	homozygous	130119622
20	46070522	46070523	A	G	57	GENIC	homozygous	130119623