chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	83984212	83984213	T	A	34	GENIC	homozygous	113501696
14	83984225	83984226	T	G	36	GENIC	homozygous	113501698
14	83984231	83984232	C	G	36	GENIC	homozygous	113501700
14	83984235	83984236	T	A	36	GENIC	homozygous	113501702
14	83984241	83984242	T	G	32	GENIC	homozygous	113501704
14	83984242	83984243	G	C	32	GENIC	homozygous	113501706
14	83984244	83984245	A	G	32	GENIC	homozygous	113501708
14	83984246	83984247	T	C	32	GENIC	homozygous	113501710
14	83984248	83984249	T	G	32	GENIC	homozygous	113501712
14	83984251	83984252	A	C	32	GENIC	homozygous	113501714
14	83984259	83984260	T	G	29	GENIC	homozygous	113501716
14	83984262	83984263	T	A	32	GENIC	homozygous	113501718
14	83989509	83989510	G	A	19	GENIC	homozygous	114056904
14	84051998	84051999	T	G	5	GENIC	homozygous	114091555
14	84090553	84090554	G	A	19	GENIC	homozygous	113501720
14	84090568	84090569	G	T	22	GENIC	homozygous	113501722
14	84090650	84090651	G	C	22	GENIC	homozygous	113501724
14	84090670	84090671	T	C	20	GENIC	homozygous	113501726
14	84090690	84090691	C	A	20	GENIC	possibly homozygous	113501727
14	84090729	84090730	A	G	26	GENIC	homozygous	113501729
14	84090730	84090731	G	A	26	GENIC	homozygous	113501731
14	84090780	84090781	G	A	22	GENIC	homozygous	113501733
14	84090973	84090974	C	A	30	GENIC	homozygous	113605400