chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	10520812	10520813	C	T	37	GENIC	homozygous	113783680
14	10521155	10521156	A	C	29	GENIC	homozygous	113783682
14	10521716	10521717	G	A	36	GENIC	homozygous	113338122
14	10521898	10521899	A	G	34	GENIC	homozygous	113338124
14	10522157	10522158	C	T	33	GENIC	homozygous	113783684
14	10522325	10522326	G	T	30	GENIC	homozygous	113338128
14	10522705	10522706	C	T	22	GENIC	homozygous	113338130
14	10523160	10523161	A	G	28	GENIC	homozygous	113338132
14	10523263	10523264	T	C	24	GENIC	homozygous	113338134
14	10524459	10524460	G	A	14	GENIC	homozygous	113338138
14	10525536	10525537	G	A	19	GENIC	homozygous	113783686
14	10525541	10525542	C	G	19	GENIC	homozygous	113338144
14	10525651	10525652	T	C	22	GENIC	homozygous	113783688
14	10525898	10525899	C	T	27	GENIC	homozygous	113783690
14	10523833	10523834	T	C	31	GENIC	heterozygous	118794114
14	10521773	10521774	G	A	19	GENIC	possibly homozygous	113649348
14	10521807	10521808	C	T	29	GENIC	possibly homozygous	113962627