chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	85733189	85733190	C	T	9	GENIC	homozygous	66544752
14	85734541	85734542	G	T	19	GENIC	homozygous	66544753
14	85735100	85735101	A	G	7	GENIC	homozygous	66544754
14	85737365	85737366	T	C	37	GENIC	heterozygous	66544755
14	85739036	85739037	A	G	15	GENIC	homozygous	66544756
14	85742444	85742445	G	A	17	GENIC	homozygous	66544757
14	85743805	85743806	A	C	9	GENIC	homozygous	66544758
14	85745081	85745082	G	A	14	GENIC	homozygous	67588171
14	85745102	85745103	A	G	14	GENIC	heterozygous	66544759
14	85745251	85745252	A	C	16	GENIC	homozygous	67513933
14	85745256	85745257	A	G	16	GENIC	homozygous	66544760
14	85745264	85745265	C	T	16	GENIC	homozygous	66544761
14	85745756	85745757	C	T	6	GENIC	homozygous	66544762
14	85746360	85746361	T	C	6	GENIC	homozygous	66544763
14	85748271	85748272	C	G	10	GENIC	homozygous	66544764
14	85748755	85748756	A	G	7	GENIC	homozygous	66544765
14	85751864	85751865	A	G	8	GENIC	homozygous	66106655
14	85752703	85752704	T	C	10	GENIC	possibly homozygous	66544766
14	85754014	85754015	T	C	20	GENIC	homozygous	66544767
14	85755867	85755868	G	T	17	GENIC	homozygous	66544768
14	85757935	85757936	C	T	15	GENIC	homozygous	66544769
14	85758260	85758261	G	A	4	GENIC	homozygous	66544770
14	85758623	85758624	G	C	3	GENIC	homozygous	66544771