chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	22665528	22665529	C	G	6	GENIC	homozygous	115469615
12	22668860	22668861	A	G	13	GENIC	homozygous	115366993
12	22665975	22665976	G	A	10	GENIC	homozygous	115366985
12	22667498	22667499	A	G	23	GENIC	homozygous	115366987
12	22667920	22667921	A	G	12	GENIC	homozygous	115366989
12	22667955	22667956	C	T	17	GENIC	homozygous	115366991
12	22666265	22666265		CTAA	15	GENIC	homozygous	131115109
12	22666423	22666423		AGGCTTGTAC	16	GENIC	homozygous	131115110
12	22669829	22669833	CTTT		6	GENIC	homozygous	131115112
12	22669934	22669935	C	T	13	GENIC	homozygous	115366995
12	22670322	22670323	G	T	15	GENIC	homozygous	115366997
12	22670586	22670587	A	G	20	GENIC	homozygous	115366999
12	22670638	22670639	C	T	24	GENIC	homozygous	115367001
12	22670674	22670675	G	A	20	GENIC	homozygous	115367003
12	22670866	22670867	C	T	15	GENIC	homozygous	115367005
12	22671116	22671117	C		21	GENIC	homozygous	131115113
12	22671118	22671119	C	T	21	GENIC	homozygous	115469617
12	22675825	22675826	T	C	9	GENIC	homozygous	115367007
12	22675903	22675904	G	A	13	GENIC	homozygous	115367009
12	22675945	22675946	T	A	17	GENIC	homozygous	115367011
12	22669732	22669733	C	T	12	GENIC	homozygous	115492676
12	22671550	22671551	A	T	25	GENIC	homozygous	118261493
12	22671553	22671554	G	T	25	GENIC	homozygous	118261494