chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	9555758	9555759	A	C	26	GENIC	homozygous	113333949
14	9556810	9556811	C	T	25	GENIC	possibly homozygous	113333951
14	9556859	9556860	A	T	33	GENIC	homozygous	113333953
14	9556966	9556967	C	T	34	GENIC	homozygous	113333955
14	9556967	9556968	A	T	33	GENIC	homozygous	113333957
14	9557123	9557124	C	A	62	GENIC	homozygous	113782178
14	9557622	9557623	A	G	56	GENIC	homozygous	113333959
14	9557751	9557752	C	A	56	GENIC	homozygous	113333961
14	9557896	9557897	A	G	57	GENIC	homozygous	113333963
14	9557912	9557913	A	C	50	GENIC	homozygous	113333965
14	9558520	9558521	T	G	40	GENIC	homozygous	113333967
14	9558620	9558621	A	G	32	GENIC	homozygous	113333969
14	9558895	9558896	A	G	45	GENIC	possibly homozygous	113333971
14	9559417	9559418	T	C	31	GENIC	possibly homozygous	113333973
14	9559562	9559563	T	G	49	GENIC	homozygous	113333975
14	9559860	9559861	T	C	35	GENIC	homozygous	113333977
14	9560140	9560141	G	A	63	GENIC	homozygous	113333979
14	9560679	9560680	G	C	35	GENIC	homozygous	113333981
14	9561593	9561594	G	T	36	GENIC	homozygous	113333983
14	9561752	9561753	T	C	47	GENIC	homozygous	113333985
14	9561760	9561761	G	A	46	GENIC	homozygous	113333987