chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	16270238	16270239	A	AT	22	GENIC	possibly homozygous	48953665
14	16271559	16271560	A	G	25	GENIC	homozygous	48544550
14	16272635	16272636	A	G	33	GENIC	homozygous	48544553
14	16275804	16275805	A	G	45	GENIC	homozygous	49460502
14	16278104	16278105	T	C	23	GENIC	homozygous	48544560
14	16278732	16278733	C	T	27	GENIC	homozygous	49460503
14	16278891	16278897	TGTGTG	------	8	GENIC	heterozygous	49300669
14	16278893	16278897	TGTG	----	8	GENIC	heterozygous	49470330
14	16280591	16280592	C	CTTTTT	32	GENIC	homozygous	49300670
14	16280742	16280743	A	G	18	GENIC	homozygous	48544563
14	16282282	16282283	T	TGGA	21	GENIC	homozygous	48544566
14	16286701	16286702	G	A	39	GENIC	homozygous	49460504
14	16287084	16287085	T	C	32	GENIC	homozygous	48544576
14	16287633	16287634	G	GCTGTCAGAAT	20	GENIC	homozygous	48544577
14	16287635	16287636	G	GGA	20	GENIC	homozygous	48544578