chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	93761278	93761279	C	T	28	GENIC	possibly homozygous	109921001
2	93761634	93761635	T	C	63	GENIC	homozygous	109921003
2	93761635	93761636	G	A	63	GENIC	homozygous	109921005
2	93762375	93762376	A	G	29	GENIC	homozygous	109921007
2	93762555	93762556	A	G	57	GENIC	homozygous	109921009
2	93763266	93763267	A	T	47	GENIC	homozygous	109921011
2	93763401	93763402	T	C	38	GENIC	homozygous	109921013
2	93763709	93763710	T	C	17	GENIC	heterozygous	109921015
2	93763974	93763975	C	T	20	GENIC	homozygous	109921017
2	93764081	93764082	C	T	20	GENIC	homozygous	109921019
2	93764614	93764615	G	A	28	GENIC	possibly homozygous	109921021
2	93765274	93765275	C	T	56	GENIC	homozygous	109921023
2	93766013	93766014	T	C	21	GENIC	homozygous	109921025
2	93766017	93766018	G	C	20	GENIC	homozygous	109921027
2	93766097	93766098	C	T	34	GENIC	homozygous	109921029
2	93766200	93766201	A	T	24	GENIC	homozygous	109921031
2	93766215	93766216	A	T	26	GENIC	homozygous	109921033
2	93766232	93766233	A	G	28	GENIC	homozygous	109921035