chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	93938877	93938878	C	T	22	GENIC	homozygous	114785278
13	93942289	93942290	T	C	17	GENIC	homozygous	114785280
13	93942517	93942518	T	C	25	GENIC	homozygous	114430016
13	93943836	93943837	A	G	14	GENIC	homozygous	114785282
13	93943881	93943882	C	T	16	GENIC	homozygous	114430022
13	93943893	93943894	T	C	18	GENIC	homozygous	114430024
13	93945210	93945211	A	G	29	GENIC	homozygous	114430028
13	93945686	93945687	C	T	26	GENIC	homozygous	114430030
13	93946242	93946243	A	G	32	GENIC	homozygous	114430034
13	93948667	93948668	A	G	20	GENIC	homozygous	114430040
13	93949170	93949171	T	G	40	GENIC	homozygous	114785284
13	93950724	93950725	C	T	26	GENIC	homozygous	114785286
13	93953087	93953088	G	C	17	GENIC	homozygous	114430048
13	93953965	93953966	C	G	24	GENIC	homozygous	114430056
13	93954246	93954247	G	A	34	GENIC	homozygous	114785288
13	93956775	93956776	G	C	20	GENIC	homozygous	114785290
13	93957285	93957286	G	C	43	GENIC	homozygous	114430072
13	93962701	93962702	G	T	10	GENIC	homozygous	114430090