chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3588535	3588536	T	C	58	GENIC	homozygous	109417284
20	3588750	3588751	C	A	68	GENIC	homozygous	109069138
20	3589590	3589591	G	A	51	GENIC	homozygous	109231776
20	3590094	3590095	T	C	74	GENIC	homozygous	109069140
20	3590143	3590144	G	A	70	GENIC	homozygous	109069142
20	3590404	3590405	C	T	56	GENIC	homozygous	109069144
20	3590774	3590775	T	C	70	GENIC	homozygous	109069146
20	3592538	3592539	C	T	67	GENIC	homozygous	109069150
20	3592811	3592812	C	T	75	GENIC	homozygous	109069152
20	3593072	3593073	G	A	45	GENIC	homozygous	109069154
20	3593180	3593181	T	C	64	GENIC	homozygous	109069156
20	3593664	3593665	T	C	57	GENIC	homozygous	109069158
20	3593829	3593830	G	A	78	GENIC	possibly homozygous	109417286
20	3595833	3595834	A	G	79	GENIC	homozygous	109069160
20	3596032	3596033	C	T	73	GENIC	homozygous	109231782
20	3597659	3597660	T	C	61	GENIC	homozygous	109069164
20	3599370	3599371	G	A	80	GENIC	homozygous	109417288
20	3591747	3591748	C	T	21	GENIC	homozygous	109328530
20	3594224	3594224		TTTG	33	GENIC	possibly homozygous	131227050
20	3590692	3590692		CC	60	GENIC	homozygous	129650956
20	3592671	3592672	T		64	GENIC	homozygous	129650957
20	3592849	3592850	C		59	GENIC	homozygous	129650958