chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3588580	3588581	G	A	12	GENIC	homozygous	109231775
20	3588750	3588751	C	A	13	GENIC	homozygous	109069138
20	3589830	3589831	T	A	23	GENIC	homozygous	109231777
20	3590094	3590095	T	C	23	GENIC	homozygous	109069140
20	3590143	3590144	G	A	8	GENIC	homozygous	109069142
20	3590404	3590405	C	T	13	GENIC	homozygous	109069144
20	3590530	3590531	C	T	9	GENIC	homozygous	109231778
20	3590774	3590775	T	C	9	GENIC	homozygous	109069146
20	3591286	3591287	C	T	12	GENIC	homozygous	109231779
20	3592538	3592539	C	T	27	GENIC	homozygous	109069150
20	3592811	3592812	C	T	17	GENIC	homozygous	109069152
20	3593180	3593181	T	C	11	GENIC	homozygous	109069156
20	3593664	3593665	T	C	11	GENIC	homozygous	109069158
20	3593819	3593820	C	T	22	GENIC	homozygous	109231780
20	3595280	3595281	G	A	5	GENIC	homozygous	109231781
20	3595833	3595834	A	G	16	GENIC	homozygous	109069160
20	3596032	3596033	C	T	17	GENIC	homozygous	109231782
20	3597659	3597660	T	C	16	GENIC	homozygous	109069164
20	3591747	3591748	C	T	8	GENIC	homozygous	109328530