chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	82954967	82954968	G	A	12	GENIC	heterozygous	133667270
3	83037581	83037582	G		16	GENIC	homozygous	127902097
3	83037608	83037608		A	14	GENIC	homozygous	127902098
3	83037623	83037624	C		15	GENIC	homozygous	127902099
3	83037636	83037636		C	13	GENIC	homozygous	127902100
3	83037650	83037650		T	12	GENIC	homozygous	127902101
3	83037657	83037657		C	11	GENIC	homozygous	127902102
3	83037680	83037681	G		14	GENIC	homozygous	127902103
3	83037686	83037687	A		13	GENIC	homozygous	127902104
3	83037702	83037703	A		12	GENIC	homozygous	127902105
3	83037726	83037727	G		11	GENIC	homozygous	127902106
3	83037782	83037783	G	A	14	GENIC	homozygous	111953266
3	83037783	83037784	A	C	14	GENIC	homozygous	111953268
3	83037796	83037796		T	17	GENIC	homozygous	127902107
3	83037867	83037868	T		21	GENIC	homozygous	127902108
3	83037873	83037873		T	21	GENIC	homozygous	127902109
3	83037909	83037910	G		23	GENIC	homozygous	127902110
3	83037918	83037919	G		23	GENIC	homozygous	127902111
3	83037977	83037977		GGG	18	GENIC	homozygous	127902112
3	83037988	83037988		A	19	GENIC	homozygous	127902113
3	83037989	83037990	A	G	19	GENIC	homozygous	119650410
3	83037997	83037997		G	19	GENIC	homozygous	127902114
3	83038049	83038049		C	19	GENIC	homozygous	127902115
3	83038052	83038053	G	T	19	GENIC	homozygous	119650411
3	83038056	83038057	T		18	GENIC	homozygous	127902116
3	83038063	83038064	G		19	GENIC	homozygous	127902117
3	83038071	83038073	CA		20	GENIC	homozygous	127902118
3	83038075	83038075		TCT	21	GENIC	homozygous	127902119