chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	44645072	44645073	G	A	44	GENIC	homozygous	113444753
14	44645194	44645195	A	C	35	GENIC	homozygous	113444755
14	44648712	44648713	C	G	39	GENIC	homozygous	113444757
14	44655287	44655288	C	T	25	GENIC	homozygous	113444759
14	44655810	44655811	A	G	29	GENIC	homozygous	113444761
14	44658543	44658544	A	G	26	GENIC	homozygous	113444763
14	44658889	44658890	T	A	34	GENIC	homozygous	113444765
14	44663095	44663096	T	A	6	GENIC	heterozygous	113444767
14	44664659	44664660	C	T	10	GENIC	homozygous	113444769
14	44664666	44664667	T	C	11	GENIC	possibly homozygous	113444771
14	44664739	44664740	A	G	19	GENIC	homozygous	113444773
14	44666291	44666292	A	C	21	GENIC	possibly homozygous	113444775
14	44671298	44671299	G	A	40	GENIC	homozygous	113444777
14	44675626	44675627	T	A	23	GENIC	homozygous	113444779
14	44677479	44677480	A	G	20	GENIC	homozygous	113444781
14	44681101	44681102	A	G	42	GENIC	homozygous	113444783
14	44683043	44683044	C	T	45	GENIC	homozygous	113444785
14	44683160	44683161	T	A	45	GENIC	homozygous	113444787
14	44685356	44685357	C	T	58	GENIC	homozygous	113444789
14	44685558	44685559	A	G	29	GENIC	possibly homozygous	113444791
14	44687543	44687544	G	T	37	GENIC	homozygous	113444793
14	44689787	44689788	T	A	16	GENIC	homozygous	113444795
14	44690823	44690824	A	G	29	GENIC	homozygous	113444797
14	44691060	44691061	A	G	56	GENIC	homozygous	113444799
14	44691371	44691372	G	A	32	GENIC	homozygous	113444801
14	44692391	44692392	C	T	17	GENIC	homozygous	113444803
14	44695698	44695699	C	T	44	GENIC	homozygous	113444805
14	44696008	44696009	A	G	32	GENIC	homozygous	113444807
14	44698227	44698228	T	C	58	GENIC	homozygous	113444809
14	44698473	44698474	G	A	56	GENIC	homozygous	113444811