chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3588535	3588536	T	C	27	GENIC	homozygous	109417284
20	3588750	3588751	C	A	16	GENIC	homozygous	109069138
20	3589590	3589591	G	A	19	GENIC	possibly homozygous	109231776
20	3590094	3590095	T	C	20	GENIC	homozygous	109069140
20	3590143	3590144	G	A	17	GENIC	homozygous	109069142
20	3590404	3590405	C	T	19	GENIC	homozygous	109069144
20	3590774	3590775	T	C	15	GENIC	homozygous	109069146
20	3591747	3591748	C	T	8	GENIC	homozygous	109328530
20	3592538	3592539	C	T	29	GENIC	homozygous	109069150
20	3592811	3592812	C	T	16	GENIC	homozygous	109069152
20	3593072	3593073	G	A	13	GENIC	homozygous	109069154
20	3593180	3593181	T	C	13	GENIC	homozygous	109069156
20	3593664	3593665	T	C	21	GENIC	possibly homozygous	109069158
20	3593829	3593830	G	A	25	GENIC	homozygous	109417286
20	3595833	3595834	A	G	24	GENIC	homozygous	109069160
20	3596032	3596033	C	T	26	GENIC	homozygous	109231782
20	3597659	3597660	T	C	18	GENIC	homozygous	109069164
20	3599370	3599371	G	A	18	GENIC	homozygous	109417288
20	3590692	3590692		CC	12	GENIC	homozygous	129650956
20	3592671	3592672	T		16	GENIC	homozygous	129650957
20	3592849	3592850	C		14	GENIC	homozygous	129650958
20	3591810	3591812	CA		3	GENIC	heterozygous	132367617
20	3591815	3591816	T	G	3	GENIC	heterozygous	132368668
20	3594224	3594224		TTTG	16	GENIC	homozygous	131227050