chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	6673686	6673687	T	A	22	GENIC	possibly homozygous	114095867
14	6673940	6673941	T	G	23	GENIC	possibly homozygous	113323349
14	6674006	6674007	A	C	24	GENIC	possibly homozygous	113323350
14	6674077	6674078	A	T	32	GENIC	possibly homozygous	113323351
14	6674792	6674793	G	A	39	GENIC	homozygous	113323353
14	6675300	6675301	G	A	28	GENIC	homozygous	113906077
14	6675650	6675651	C	T	13	GENIC	homozygous	113571697
14	6675800	6675801	G	A	21	GENIC	homozygous	113571698
14	6676024	6676025	A	G	25	GENIC	homozygous	113571699
14	6676046	6676047	T	C	20	GENIC	homozygous	113571700
14	6676206	6676207	G	C	20	GENIC	homozygous	114095868
14	6676220	6676221	T	C	19	GENIC	homozygous	113571701
14	6676544	6676545	G	C	14	GENIC	homozygous	113571702
14	6676702	6676703	T	C	26	GENIC	homozygous	113571703
14	6676884	6676885	A	T	20	GENIC	homozygous	113571704
14	6676938	6676939	C	T	19	GENIC	homozygous	113571706
14	6677197	6677198	T	C	16	GENIC	homozygous	113571707
14	6677211	6677212	G	C	14	GENIC	homozygous	113571708
14	6677212	6677213	T	A	14	GENIC	homozygous	113571709
14	6677482	6677483	T	C	33	GENIC	homozygous	113571710
14	6677509	6677510	A	G	31	GENIC	homozygous	113571711
14	6677595	6677596	G	T	28	GENIC	homozygous	113571712
14	6677870	6677871	A	G	18	GENIC	homozygous	113571713
14	6677961	6677962	T	C	21	GENIC	homozygous	113571714
14	6678183	6678184	T	G	26	GENIC	possibly homozygous	113571715
14	6678277	6678278	C	G	20	GENIC	possibly homozygous	113571716
14	6678378	6678379	A	G	22	GENIC	homozygous	113571717
14	6678604	6678605	C	A	21	GENIC	homozygous	113571718
14	6678608	6678609	G	C	21	GENIC	homozygous	113802646
14	6678672	6678673	T	C	22	GENIC	homozygous	113571719
14	6678796	6678797	C	T	23	GENIC	homozygous	113571720
14	6678809	6678810	G	T	18	GENIC	homozygous	113571721
14	6678819	6678820	C	A	21	GENIC	homozygous	113571722
14	6678832	6678833	G	T	22	GENIC	homozygous	113571723
14	6679803	6679804	C	T	26	GENIC	homozygous	113571725
14	6679948	6679949	T	C	18	GENIC	homozygous	113571726