chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	87393805	87393806	T	-	11	GENIC	heterozygous	49292287
14	87398084	87398085	G	GT	31	GENIC	homozygous	49316796
14	87398086	87398087	C	CTGCCTGGGCCACTGCAG	32	GENIC	homozygous	49316797
14	87401944	87401945	A	AACACTTACATG	38	GENIC	homozygous	48814657
14	87406685	87406686	T	A	22	GENIC	homozygous	48814663
14	87406707	87406708	C	T	17	GENIC	homozygous	48814665
14	87406709	87406710	A	T	14	GENIC	homozygous	48814667
14	87406711	87406712	G	T	14	GENIC	homozygous	48814669
14	87406716	87406717	A	T	14	GENIC	homozygous	48814671
14	87406725	87406726	A	AT	17	GENIC	homozygous	48814673
14	87406734	87406735	C	CT	21	GENIC	homozygous	48814675
14	87415613	87415614	T	-	12	GENIC	heterozygous	49421383
14	87422703	87422704	T	-	17	GENIC	heterozygous	49327757
14	87425527	87425528	T	C	21	GENIC	heterozygous	49023318
14	87427076	87427077	G	-	4	GENIC	heterozygous	49327758
14	87429670	87429671	G	-	6	GENIC	homozygous	48814694
14	87430786	87430787	C	CATAGATAG	8	GENIC	homozygous	49397703
14	87439640	87439641	A	-	9	GENIC	heterozygous	49332124