chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	93761004	93761005	C	T	13	GENIC	homozygous	110720556
2	93761634	93761635	T	C	30	GENIC	homozygous	109921003
2	93761635	93761636	G	A	30	GENIC	homozygous	109921005
2	93762341	93762342	A	G	11	GENIC	homozygous	110720557
2	93763266	93763267	A	T	23	GENIC	homozygous	109921011
2	93763401	93763402	T	C	29	GENIC	homozygous	109921013
2	93763974	93763975	C	T	12	GENIC	homozygous	109921017
2	93764081	93764082	C	T	7	GENIC	homozygous	109921019
2	93764184	93764185	G	A	8	GENIC	homozygous	110720558
2	93765274	93765275	C	T	40	GENIC	homozygous	109921023
2	93765466	93765467	C	T	20	GENIC	homozygous	110720559
2	93766013	93766014	T	C	15	GENIC	homozygous	109921025
2	93766017	93766018	G	C	16	GENIC	homozygous	109921027
2	93766097	93766098	C	T	23	GENIC	homozygous	109921029
2	93766200	93766201	A	T	20	GENIC	homozygous	109921031
2	93766215	93766216	A	T	19	GENIC	homozygous	109921033
2	93766232	93766233	A	G	18	GENIC	homozygous	109921035