chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95286762	95286763	T	C	49	GENIC	homozygous	117392236
9	95291196	95291197	T	C	34	GENIC	homozygous	117392240
9	95291607	95291608	T	C	41	GENIC	homozygous	117392242
9	95291766	95291767	A	G	28	GENIC	homozygous	117392244
9	95293121	95293122	C	T	44	GENIC	homozygous	117392246
9	95293235	95293236	A	G	48	GENIC	homozygous	117392248
9	95295006	95295007	G	T	35	GENIC	homozygous	117392250
9	95295532	95295533	G	A	25	GENIC	homozygous	117392251
9	95295613	95295614	C	G	37	GENIC	homozygous	117392253
9	95296496	95296497	C	T	52	GENIC	homozygous	117392255
9	95297143	95297144	A	G	46	GENIC	homozygous	117392257
9	95297677	95297678	T	A	38	GENIC	homozygous	117392259
9	95297885	95297886	A	G	40	GENIC	homozygous	117392261
9	95298065	95298066	G	T	47	GENIC	homozygous	117392263
9	95298086	95298087	A	G	38	GENIC	homozygous	117392264
9	95298115	95298116	G	A	32	GENIC	homozygous	117392266
9	95298157	95298158	G	C	34	GENIC	homozygous	117392268
9	95298171	95298172	C	T	35	GENIC	homozygous	117392270
9	95298823	95298824	T	C	52	GENIC	homozygous	117392272
9	95299494	95299495	T	C	49	GENIC	homozygous	117392273
9	95299505	95299506	G	C	57	GENIC	homozygous	117392275
9	95300043	95300044	C	T	27	GENIC	homozygous	117392277
9	95302314	95302315	A	T	21	GENIC	homozygous	117392278
9	95302741	95302742	A	G	27	GENIC	homozygous	117392280