chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	107767881	107767882	G	A	35	GENIC	homozygous	113618066
14	107767883	107767884	T	C	36	GENIC	homozygous	113539508
14	107768752	107768753	A	G	31	GENIC	homozygous	113618067
14	107770637	107770638	C	A	19	GENIC	homozygous	113828092
14	107770796	107770797	A	G	19	GENIC	homozygous	113828094
14	107770956	107770957	T	C	29	GENIC	homozygous	113828096
14	107772110	107772111	T	C	34	GENIC	homozygous	113828098
14	107773426	107773427	C	T	30	GENIC	homozygous	113618071
14	107774417	107774418	T	C	36	GENIC	homozygous	113828100
14	107774712	107774713	T	A	35	GENIC	homozygous	113828102
14	107775347	107775348	A	C	36	GENIC	homozygous	113828104
14	107775960	107775961	A	G	34	GENIC	homozygous	113828106
14	107776309	107776310	T	C	25	GENIC	homozygous	113828108
14	107776903	107776904	A	G	27	GENIC	homozygous	113828110
14	107777200	107777201	G	A	27	GENIC	homozygous	113828112
14	107777206	107777207	C	T	32	GENIC	homozygous	113828114
14	107779826	107779827	C	T	30	GENIC	homozygous	113828116