chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	87457715	87457715		T	59	GENIC	homozygous	129179883
14	87460907	87460908	T		47	GENIC	homozygous	129179885
14	87461892	87461893	T	C	55	GENIC	homozygous	113502115
14	87457893	87457894	G	A	44	GENIC	homozygous	113502107
14	87460634	87460635	C	T	48	GENIC	homozygous	113502109
14	87461643	87461644	G	A	50	GENIC	homozygous	113502111
14	87461720	87461721	G	A	47	GENIC	possibly homozygous	113502113
14	87462202	87462203	C	T	40	GENIC	homozygous	113502117
14	87463067	87463068	C	T	49	GENIC	homozygous	113502119
14	87463756	87463757	A	T	48	GENIC	homozygous	113502121
14	87463950	87463951	C	T	55	GENIC	homozygous	113502123
14	87464910	87464911	C	T	49	GENIC	homozygous	113502125
14	87465095	87465095		CTCCGT	28	GENIC	homozygous	129179886
14	87465167	87465167		G	23	GENIC	homozygous	129179887
14	87465180	87465180		C	24	GENIC	homozygous	129179888
14	87465190	87465190		C	24	GENIC	homozygous	129179889