chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	15723025	15723026	A	G	58	GENIC	homozygous	139459017
14	15723136	15723137	C	T	40	GENIC	homozygous	139459018
14	15723139	15723140	C	T	41	GENIC	homozygous	139459019
14	15723338	15723339	A	T	64	GENIC	homozygous	139459020
14	15723917	15723918	G		40	GENIC	possibly homozygous	403653075
14	15723917	15723918	G	C	40	GENIC	heterozygous	403653076
14	15723919	15723920	C	G	40	GENIC	heterozygous	154826186
14	15723919	15723920	C		40	GENIC	possibly homozygous	403851079
14	15723923	15723924	C		40	GENIC	possibly homozygous	403851080
14	15723923	15723924	C	G	40	GENIC	heterozygous	403851081
14	15724783	15724784	T	C	33	GENIC	homozygous	139459021
14	15725194	15725195	T	A	56	GENIC	homozygous	139459022
14	15725496	15725497	T	C	58	GENIC	homozygous	139459023
14	15726637	15726638	G	A	56	GENIC	homozygous	139459027
14	15725653	15725654	T	G	31	GENIC	homozygous	139459024
14	15726494	15726495	C	T	41	GENIC	homozygous	139459025
14	15726537	15726538	T	G	43	GENIC	homozygous	139459026
14	15726857	15726858	T	C	45	GENIC	homozygous	139459028
14	15726866	15726867	C	T	47	GENIC	homozygous	139459029
14	15727734	15727735	G	A	65	GENIC	homozygous	139459030
14	15725859	15725863	TATG		16	GENIC	homozygous	139381166
14	15725842	15725842		AT	16	GENIC	homozygous	139381165