chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	107767881	107767882	G	A	16	GENIC	homozygous	113618066
14	107767883	107767884	T	C	16	GENIC	homozygous	113539508
14	107768752	107768753	A	G	25	GENIC	homozygous	113618067
14	107769187	107769188	G	A	31	GENIC	homozygous	113618068
14	107770521	107770522	C	T	29	GENIC	homozygous	113618069
14	107772898	107772899	G	A	39	GENIC	possibly homozygous	113618070
14	107773426	107773427	C	T	13	GENIC	homozygous	113618071
14	107773435	107773436	T	C	11	GENIC	homozygous	113618072
14	107775101	107775102	G	A	14	GENIC	homozygous	113618073
14	107778330	107778331	G	A	19	GENIC	homozygous	113618075
14	107778137	107778138	G	A	20	GENIC	homozygous	113694966