chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	22786917	22786918	T	C	41	GENIC	homozygous	113723470
14	22787276	22787277	C	G	41	GENIC	homozygous	113723472
14	22787828	22787829	A	C	42	GENIC	homozygous	113723474
14	22787873	22787874	A	G	28	GENIC	homozygous	113383833
14	22788063	22788064	A	G	40	GENIC	homozygous	113723476
14	22788140	22788141	T	A	49	GENIC	homozygous	113723478
14	22788255	22788256	T	C	36	GENIC	possibly homozygous	113383835
14	22788405	22788406	C	T	49	GENIC	homozygous	113723480
14	22788426	22788427	G	T	53	GENIC	homozygous	113723482
14	22788723	22788724	T	C	34	GENIC	homozygous	114121308
14	22789071	22789072	G	C	108	GENIC	heterozygous	118750012
14	22788285	22788286	T	C	30	GENIC	homozygous	113784838
14	22788557	22788558	T	G	55	GENIC	homozygous	113784840
14	22788726	22788727	G	A	35	GENIC	possibly homozygous	118750009
14	22788735	22788736	G	C	37	GENIC	possibly homozygous	118750010
14	22788818	22788819	A	G	32	GENIC	heterozygous	118750011
14	22791192	22791193	C	T	128	GENIC	heterozygous	118801840
14	22791284	22791285	C	T	97	GENIC	heterozygous	118801842
14	22791336	22791337	C	T	117	GENIC	heterozygous	118836051
14	22791338	22791339	T	A	119	GENIC	heterozygous	118836052
14	22791406	22791407	C	T	137	GENIC	heterozygous	118836053
14	22789527	22789528	C	G	201	GENIC	heterozygous	118683803
14	22790885	22790886	A	C	155	GENIC	heterozygous	118683804
14	22795153	22795154	C	T	42	GENIC	homozygous	118750016