chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	14020093	14020094	C	T	54	GENIC	homozygous	109100590
20	14020276	14020277	A	C	38	GENIC	homozygous	109100592
20	14020306	14020307	C	T	24	GENIC	homozygous	109492792
20	14021440	14021441	T	C	55	GENIC	homozygous	109100594
20	14022347	14022348	C	T	56	GENIC	possibly homozygous	109100596
20	14023440	14023441	G	A	43	GENIC	homozygous	109100598
20	14023912	14023913	A	G	19	GENIC	heterozygous	119815833
20	14025516	14025517	T	C	3	GENIC	homozygous	119771181
20	14025819	14025820	G	C	54	GENIC	possibly homozygous	109100600
20	14027976	14027977	G	T	18	GENIC	homozygous	109302790
20	14028441	14028442	C	A	43	GENIC	homozygous	119771183
20	14028694	14028695	A	G	6	GENIC	homozygous	119771185
20	14036766	14036767	C	T	28	GENIC	homozygous	109331929
20	14036770	14036771	T	C	28	GENIC	homozygous	109331931
20	14036787	14036788	T	G	42	GENIC	homozygous	109331933
20	14037026	14037027	G	C	39	GENIC	homozygous	119771187
20	14037085	14037086	C	T	55	GENIC	homozygous	109240703
20	14037194	14037195	A	T	28	GENIC	homozygous	109394308
20	14037195	14037196	C	G	28	GENIC	homozygous	119771189
20	14037811	14037812	C	T	31	GENIC	homozygous	119771191
20	14041684	14041685	T	G	28	GENIC	homozygous	109302794
20	14045747	14045748	T	G	79	GENIC	heterozygous	109542909