chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	14081428	14081429	T	C	52	GENIC	homozygous	109302821
20	14082539	14082540	T	C	36	GENIC	homozygous	109100671
20	14083784	14083785	A	G	46	GENIC	possibly homozygous	109100673
20	14085192	14085193	C	A	42	GENIC	possibly homozygous	119771210
20	14085529	14085530	T	C	14	GENIC	homozygous	119771212
20	14088016	14088017	C	T	56	GENIC	homozygous	109302823
20	14088787	14088788	A	G	43	GENIC	possibly homozygous	109240712
20	14088845	14088846	A	G	43	GENIC	homozygous	109100681
20	14088856	14088857	T	C	38	GENIC	homozygous	109302825
20	14088915	14088916	T	C	52	GENIC	homozygous	109100685
20	14088944	14088945	G	C	57	GENIC	homozygous	109302827
20	14089321	14089322	T	C	37	GENIC	possibly homozygous	119882184
20	14089771	14089772	C	T	67	GENIC	homozygous	109302829
20	14089976	14089977	A	C	46	GENIC	possibly homozygous	109100687
20	14090658	14090659	A	G	60	GENIC	homozygous	109100689
20	14092698	14092699	T	G	61	GENIC	possibly homozygous	109100691