chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	90615657	90615658	C	T	44	GENIC	homozygous	138373618
8	90616365	90616366	T	C	32	GENIC	homozygous	146881928
8	90616677	90616678	C	T	45	GENIC	homozygous	146881929
8	90616889	90616890	G	C	31	GENIC	homozygous	146881930
8	90617440	90617441	T	C	20	GENIC	homozygous	138373619
8	90620039	90620040	G	A	46	GENIC	homozygous	138373620
8	90621323	90621323		G	66	GENIC	homozygous	138255072
8	90622411	90622412	G	A	42	GENIC	homozygous	146881931
8	90622461	90622462	G	C	36	GENIC	homozygous	146881932
8	90622725	90622726	G	T	37	GENIC	homozygous	146881933
8	90623773	90623774	A	G	59	GENIC	homozygous	138373623
8	90625399	90625400	T		38	GENIC	homozygous	138255073
8	90626211	90626212	T		42	GENIC	possibly homozygous	138255074
8	90627055	90627056	G	A	65	GENIC	homozygous	146881934
8	90627383	90627384	C	G	42	GENIC	homozygous	138373624
8	90627559	90627560	C	T	44	GENIC	homozygous	146881935
8	90625586	90625586		T	56	GENIC	homozygous	146847349