chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	15288698	15288699	A	G	51	GENIC	homozygous	45444932
20	15288817	15288818	C	CT	19	GENIC	heterozygous	45444934
20	15288817	15288818	C	CTT	19	GENIC	heterozygous	45444936
20	15288817	15288818	C	CTTTTTT	19	GENIC	heterozygous	45444938
20	15289126	15289127	G	-	41	GENIC	homozygous	45444941
20	15289917	15289918	G	A	51	GENIC	homozygous	45444943
20	15290008	15290009	C	G	46	GENIC	heterozygous	45444945
20	15290025	15290026	T	G	37	GENIC	homozygous	45444947
20	15290069	15290070	C	T	44	GENIC	possibly homozygous	45444949
20	15290237	15290238	T	-	26	GENIC	homozygous	45444951
20	15290310	15290311	G	A	38	GENIC	homozygous	45444953
20	15290406	15290407	T	C	37	GENIC	homozygous	45444955
20	15291186	15291187	T	TA	16	GENIC	heterozygous	45444957
20	15291199	15291200	G	-	22	GENIC	heterozygous	45444959
20	15291242	15291243	T	C	46	GENIC	possibly homozygous	45444961
20	15291761	15291762	T	A	43	GENIC	homozygous	45444963
20	15291771	15291773	TT	--	37	GENIC	homozygous	45444965
20	15291805	15291806	T	C	37	GENIC	homozygous	45444967
20	15292198	15292199	A	T	47	GENIC	homozygous	45444969
20	15292211	15292212	T	-	42	GENIC	homozygous	45444972
20	15292629	15292630	C	-	6	GENIC	homozygous	45444974
20	15293319	15293320	A	AAAG	16	GENIC	possibly homozygous	45444976
20	15293758	15293759	A	T	37	GENIC	homozygous	45444978
20	15293932	15293933	C	T	43	GENIC	homozygous	45444980
20	15294021	15294022	T	C	47	GENIC	possibly homozygous	45444982
20	15294349	15294350	C	CGT	16	GENIC	homozygous	45444984
20	15294519	15294520	G	A	18	GENIC	heterozygous	45444986
20	15295729	15295730	G	A	38	GENIC	homozygous	45444988
20	15295855	15295856	T	-	30	GENIC	homozygous	45444990
20	15296191	15296192	G	A	48	GENIC	homozygous	45444992
20	15296278	15296279	C	A	55	GENIC	homozygous	45444994
20	15296335	15296336	C	T	48	GENIC	homozygous	45444996