chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93940117	93940118	A	G	19	GENIC	homozygous	114971072
13	93942289	93942290	T	C	13	GENIC	homozygous	114785280
13	93942983	93942984	G	A	5	GENIC	homozygous	114430018
13	93943881	93943882	C	T	20	GENIC	homozygous	114430022
13	93944600	93944601	C	T	23	GENIC	homozygous	114971074
13	93945040	93945041	G	A	30	GENIC	homozygous	114971076
13	93945686	93945687	C	T	24	GENIC	homozygous	114430030
13	93946242	93946243	A	G	21	GENIC	homozygous	114430034
13	93947144	93947145	C	T	27	GENIC	homozygous	114971078
13	93948667	93948668	A	G	25	GENIC	homozygous	114430040
13	93952385	93952386	C	T	11	GENIC	homozygous	114971080
13	93953087	93953088	G	C	13	GENIC	homozygous	114430048
13	93953438	93953439	C	T	20	GENIC	homozygous	114430050
13	93953481	93953482	A	G	23	GENIC	homozygous	114430052
13	93953485	93953486	T	C	22	GENIC	homozygous	114430054
13	93954246	93954247	G	A	22	GENIC	homozygous	114785288
13	93957285	93957286	G	C	26	GENIC	homozygous	114430072
13	93957522	93957523	C	T	24	GENIC	homozygous	114971082
13	93957857	93957858	C	T	26	GENIC	homozygous	114971084
13	93958423	93958424	A	C	17	GENIC	homozygous	114430078
13	93959130	93959131	G	A	17	GENIC	homozygous	114971086
13	93959529	93959530	A	G	25	GENIC	homozygous	114971088
13	93961112	93961113	T	C	20	GENIC	homozygous	114971090
13	93962701	93962702	G	T	20	GENIC	homozygous	114430090
13	93954488	93954489	A	T	22	GENIC	homozygous	114988557