chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
6	20582783	20582784	G	T	24	GENIC	homozygous	54816612
6	20582939	20582940	C	T	27	GENIC	homozygous	55481555
6	20583164	20583165	C	T	38	GENIC	homozygous	54816614
6	20583321	20583322	C	T	25	GENIC	homozygous	55481557
6	20583463	20583464	T	-	24	GENIC	homozygous	55481559
6	20584292	20584293	A	G	26	GENIC	homozygous	55481561
6	20584383	20584384	A	C	28	GENIC	homozygous	55481563
6	20585431	20585432	A	G	30	GENIC	homozygous	55481565
6	20585610	20585611	A	G	36	GENIC	homozygous	54816617
6	20585696	20585697	T	C	24	GENIC	homozygous	54816618
6	20585720	20585721	T	G	26	GENIC	homozygous	54816619
6	20585792	20585793	G	A	21	GENIC	homozygous	55481567
6	20586071	20586072	T	A	25	GENIC	homozygous	54816620
6	20586198	20586199	G	-	22	GENIC	homozygous	55481569
6	20586230	20586231	G	A	22	GENIC	homozygous	55481571
6	20586425	20586426	T	C	18	GENIC	homozygous	55481573
6	20586483	20586484	T	C	20	GENIC	homozygous	55481575
6	20587315	20587316	G	T	24	GENIC	homozygous	54816621
6	20587628	20587629	T	C	34	GENIC	homozygous	55481577
6	20587967	20587968	A	G	36	GENIC	homozygous	54816622
6	20588718	20588722	TCTC	----	16	GENIC	possibly homozygous	55481579
6	20588748	20588749	A	ACG	27	GENIC	possibly homozygous	55481581
6	20588766	20588767	A	ACACACG	42	GENIC	homozygous	55481583
6	20588812	20588813	A	G	33	GENIC	homozygous	55481585
6	20589079	20589080	C	T	18	GENIC	homozygous	54816624
6	20589127	20589128	C	T	29	GENIC	homozygous	54816625
6	20589193	20589194	T	C	40	GENIC	possibly homozygous	54816626
6	20589756	20589757	C	T	31	GENIC	homozygous	55481587
6	20590357	20590358	T	A	37	GENIC	homozygous	54816627