chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3588580	3588581	G	A	39	GENIC	homozygous	109231775
20	3588750	3588751	C	A	36	GENIC	homozygous	109069138
20	3589590	3589591	G	A	15	GENIC	homozygous	109231776
20	3589830	3589831	T	A	31	GENIC	homozygous	109231777
20	3590094	3590095	T	C	28	GENIC	homozygous	109069140
20	3590143	3590144	G	A	28	GENIC	homozygous	109069142
20	3590404	3590405	C	T	38	GENIC	homozygous	109069144
20	3590530	3590531	C	T	24	GENIC	homozygous	109231778
20	3590774	3590775	T	C	24	GENIC	homozygous	109069146
20	3591286	3591287	C	T	36	GENIC	homozygous	109231779
20	3591940	3591941	G	A	19	GENIC	homozygous	109370798
20	3592538	3592539	C	T	29	GENIC	homozygous	109069150
20	3592811	3592812	C	T	21	GENIC	homozygous	109069152
20	3593072	3593073	G	A	23	GENIC	homozygous	109069154
20	3593180	3593181	T	C	25	GENIC	homozygous	109069156
20	3593664	3593665	T	C	30	GENIC	homozygous	109069158
20	3593819	3593820	C	T	30	GENIC	homozygous	109231780
20	3595280	3595281	G	A	26	GENIC	homozygous	109231781
20	3595833	3595834	A	G	27	GENIC	homozygous	109069160
20	3596032	3596033	C	T	32	GENIC	homozygous	109231782
20	3597659	3597660	T	C	23	GENIC	homozygous	109069164