chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	47075408	47075409	C	T	56	GENIC	homozygous	140565544
20	47075590	47075591	T	A	35	GENIC	homozygous	140565545
20	47075689	47075690	T		43	GENIC	homozygous	140496419
20	47075709	47075710	G	C	48	GENIC	homozygous	140565546
20	47076430	47076430		AATT	22	GENIC	homozygous	140496420
20	47076666	47076667	C	G	52	GENIC	homozygous	140565547
20	47076668	47076669	G	T	52	GENIC	homozygous	140565548
20	47076870	47076875	GTTTG		41	GENIC	possibly homozygous	140496421
20	47077008	47077009	T	C	32	GENIC	homozygous	140565549
20	47077027	47077031	CTTC		34	GENIC	homozygous	140496422
20	47077092	47077093	C	A	31	GENIC	homozygous	140565550
20	47077103	47077104	T	C	36	GENIC	homozygous	140565551
20	47077396	47077397	T	C	54	GENIC	homozygous	140565552