chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3588750	3588751	C	A	51	GENIC	homozygous	109069138
20	3590094	3590095	T	C	44	GENIC	homozygous	109069140
20	3590143	3590144	G	A	54	GENIC	homozygous	109069142
20	3590404	3590405	C	T	70	GENIC	homozygous	109069144
20	3590774	3590775	T	C	84	GENIC	homozygous	109069146
20	3591023	3591024	C	T	47	GENIC	homozygous	109069148
20	3592538	3592539	C	T	36	GENIC	possibly homozygous	109069150
20	3592811	3592812	C	T	60	GENIC	homozygous	109069152
20	3593072	3593073	G	A	49	GENIC	homozygous	109069154
20	3593180	3593181	T	C	42	GENIC	homozygous	109069156
20	3593664	3593665	T	C	50	GENIC	homozygous	109069158
20	3595833	3595834	A	G	53	GENIC	homozygous	109069160
20	3597347	3597348	C	T	54	GENIC	homozygous	109069162
20	3597659	3597660	T	C	71	GENIC	homozygous	109069164
20	3598082	3598083	A	T	51	GENIC	homozygous	109069166
20	3598528	3598529	C	T	44	GENIC	homozygous	109069168
20	3591804	3591805	G	A	27	GENIC	heterozygous	119756212
20	3591808	3591809	A	G	25	GENIC	heterozygous	109552205
20	3591747	3591748	C	T	37	GENIC	homozygous	109328530