chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	33895023	33895024	A	G	30	GENIC	homozygous	138303688
8	33895061	33895062	C	T	28	GENIC	homozygous	138303689
8	33895308	33895309	C	T	28	GENIC	homozygous	138303690
8	33895332	33895333	T	C	29	GENIC	homozygous	138303691
8	33896434	33896435	C	T	29	GENIC	homozygous	138303692
8	33896476	33896477	C	T	35	GENIC	homozygous	138303693
8	33896706	33896707	A	G	28	GENIC	homozygous	138303694
8	33896896	33896896		A	23	GENIC	homozygous	138239519
8	33897600	33897607	GACAACT		31	GENIC	homozygous	138239520
8	33897794	33897795	G	A	34	GENIC	homozygous	138303695
8	33898269	33898299	GCTCCTGCTCCTGCTCCTGCTCCTGCTCCT		19	GENIC	homozygous	138239521
8	33898519	33898520	C	T	28	GENIC	homozygous	138303696
8	33900847	33900848	C	T	22	GENIC	homozygous	138303697
8	33902577	33902578	G	A	35	GENIC	homozygous	138303698
8	33907242	33907243	G	T	8	GENIC	homozygous	138303699
8	33908367	33908368	G	A	24	GENIC	possibly homozygous	138303700
8	33899311	33899312	C		29	GENIC	homozygous	138239522
8	33903808	33903808		T	25	GENIC	homozygous	138239523
8	33906133	33906133		AAA	9	GENIC	possibly homozygous	138239524
8	33908961	33908963	CA		20	GENIC	homozygous	138239525