chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	15772219	15772220	A	T	30	GENIC	possibly homozygous	132046134
3	15772248	15772249	G	C	31	GENIC	homozygous	132046135
3	15772254	15772255	T	C	28	GENIC	homozygous	132046136
3	15772275	15772276	A	C	31	GENIC	homozygous	132046137
3	15772286	15772287	A	C	30	GENIC	homozygous	132046138
3	15772436	15772437	G	C	11	GENIC	homozygous	112068454
3	15772450	15772451	T	A	12	GENIC	homozygous	112068456
3	15772463	15772464	C	A	12	GENIC	homozygous	132046139
3	15772647	15772648	A	C	20	GENIC	homozygous	132046140
3	15772878	15772879	C	T	32	GENIC	homozygous	125886814
3	15772885	15772889	CGTC		31	GENIC	homozygous	130900853
3	15772925	15772926	C	G	30	GENIC	homozygous	132046141
3	15773010	15773011	G	T	26	GENIC	homozygous	112068460
3	15773047	15773048	C	T	32	GENIC	homozygous	125886815
3	15773186	15773187	C	T	38	GENIC	homozygous	125886816
3	15773789	15773790	T	G	6	GENIC	homozygous	132046142
3	15773859	15773860	T	A	11	GENIC	homozygous	132046143
3	15773864	15773865	T	C	12	GENIC	homozygous	132046144
3	15774084	15774085	A	G	15	GENIC	homozygous	132046145
3	15774529	15774530	A	G	22	GENIC	homozygous	132046146
3	15774669	15774669		T	35	GENIC	homozygous	132039078