chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	91933866	91933867	A	T	5	GENIC	homozygous	126124689
13	91933910	91933911	G	A	7	GENIC	homozygous	126124690
13	91934169	91934170	G	C	28	GENIC	homozygous	126124691
13	91934563	91934564	G	A	27	GENIC	homozygous	115153834
13	91935215	91935216	T	G	21	GENIC	homozygous	115153838
13	91935603	91935604	G	T	22	GENIC	homozygous	126124692
13	91935726	91935727	A	G	13	GENIC	homozygous	115153842
13	91935806	91935807	C	T	32	GENIC	homozygous	126124693
13	91939460	91939461	G	C	20	GENIC	homozygous	126124694
13	91940613	91940614	C	T	21	GENIC	homozygous	126124695
13	91943629	91943630	T	C	13	GENIC	homozygous	126124696
13	91944051	91944052	T	A	26	GENIC	homozygous	126124697
13	91945651	91945652	G	A	18	GENIC	homozygous	126124698
13	91947117	91947118	G	T	5	GENIC	homozygous	126124699
13	91947621	91947622	G	A	18	GENIC	homozygous	126124700
13	91947902	91947903	T	G	29	GENIC	homozygous	126124701
13	91948313	91948314	T	C	22	GENIC	homozygous	126124702
13	91948720	91948721	G	A	23	GENIC	homozygous	126124703
13	91949950	91949951	C	T	15	GENIC	homozygous	126124704
13	91949953	91949954	A	G	10	GENIC	heterozygous	126124705
13	91950102	91950103	G	A	12	GENIC	homozygous	126124706
13	91950459	91950460	A	G	22	GENIC	homozygous	126124707
13	91950485	91950486	A	G	15	GENIC	homozygous	126124708
13	91950544	91950545	A	G	15	GENIC	homozygous	126124709
13	91950578	91950579	G	T	13	GENIC	homozygous	126124710
13	91956920	91956921	A	G	28	GENIC	homozygous	126124711
13	91957374	91957375	C	T	5	GENIC	homozygous	126124712
13	91960563	91960564	G	A	21	GENIC	homozygous	126124713
13	91962288	91962289	A	G	18	GENIC	homozygous	126124714