chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	20606241	20606242	T	C	64	GENIC	homozygous	138288049
8	20606723	20606724	G	T	68	GENIC	homozygous	138288050
8	20607511	20607512	C	T	65	GENIC	homozygous	138288051
8	20608185	20608186	T		57	GENIC	possibly homozygous	138236227
8	20608263	20608264	C	A	58	GENIC	homozygous	138288052
8	20608685	20608687	AA		48	GENIC	homozygous	138236228
8	20608901	20608937	AGGGAGGGAGGGAGGGAGGGAGGGAGGGAGGGAGGC		21	GENIC	homozygous	138236229
8	20608954	20608955	G	A	25	GENIC	homozygous	138288053
8	20609013	20609014	A	G	43	GENIC	homozygous	138288054
8	20609241	20609242	A	G	59	GENIC	homozygous	138288055
8	20609743	20609743		ACACACAG	21	GENIC	possibly homozygous	138236230
8	20610026	20610027	A	G	48	GENIC	homozygous	138288056
8	20610206	20610208	TT		15	GENIC	homozygous	138236231
8	20610308	20610309	G	A	43	GENIC	homozygous	138288057
8	20610427	20610428	C	T	68	GENIC	homozygous	138288058
8	20610612	20610613	A	G	78	GENIC	homozygous	138288059
8	20610693	20610694	G	T	31	GENIC	possibly homozygous	138288060
8	20610697	20610700	TGT		26	GENIC	possibly homozygous	138236232
8	20610761	20610762	G	A	29	GENIC	possibly homozygous	138288061
8	20612542	20612543	A	G	65	GENIC	homozygous	138288062
8	20615566	20615566		A	58	GENIC	homozygous	138236233
8	20615698	20615699	C	T	63	GENIC	homozygous	138288063
8	20608932	20608933	G		21	GENIC	homozygous	404006283
8	20608932	20608933	G	C	21	GENIC	heterozygous	404006284