chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	9236256	9236257	C	T	26	GENIC	homozygous	130048733
20	9236491	9236492	C	G	32	GENIC	homozygous	130048736
20	9236557	9236558	G	A	30	GENIC	homozygous	130048738
20	9236610	9236611	C	A	26	GENIC	homozygous	130048741
20	9236749	9236750	T	C	20	GENIC	homozygous	130048744
20	9236802	9236803	C	T	22	GENIC	homozygous	130048747
20	9236831	9236832	C	T	20	GENIC	homozygous	130048750
20	9236844	9236845	A	G	23	GENIC	homozygous	130048752
20	9237252	9237253	C		33	GENIC	homozygous	129981972
20	9237267	9237268	C	T	33	GENIC	homozygous	130048755
20	9237280	9237281	T	C	35	GENIC	homozygous	130048758
20	9237283	9237284	A		36	GENIC	homozygous	129981973
20	9237320	9237320		CTGGCACT	33	GENIC	homozygous	129981974
20	9238391	9238392	A		9	GENIC	homozygous	129981975
20	9239233	9239234	T	C	26	GENIC	homozygous	130048761
20	9239282	9239283	T	C	26	GENIC	homozygous	130048764
20	9239292	9239293	C	G	30	GENIC	homozygous	130048767