chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	95286762	95286763	T	C	35	GENIC	homozygous	117392236
9	95287623	95287624	A	G	23	GENIC	homozygous	117392238
9	95287652	95287653	C	T	23	GENIC	homozygous	117602909
9	95290983	95290984	G	A	42	GENIC	homozygous	117602911
9	95291196	95291197	T	C	30	GENIC	homozygous	117392240
9	95291607	95291608	T	C	28	GENIC	homozygous	117392242
9	95291766	95291767	A	G	18	GENIC	homozygous	117392244
9	95293121	95293122	C	T	49	GENIC	homozygous	117392246
9	95293235	95293236	A	G	43	GENIC	homozygous	117392248
9	95295006	95295007	G	T	25	GENIC	homozygous	117392250
9	95295174	95295175	G	C	83	GENIC	heterozygous	120270655
9	95295532	95295533	G	A	28	GENIC	homozygous	117392251
9	95296496	95296497	C	T	29	GENIC	homozygous	117392255
9	95297143	95297144	A	G	29	GENIC	homozygous	117392257
9	95297313	95297314	C	T	23	GENIC	possibly homozygous	117602913
9	95297677	95297678	T	A	40	GENIC	possibly homozygous	117392259
9	95297885	95297886	A	G	35	GENIC	homozygous	117392261
9	95298065	95298066	G	T	21	GENIC	homozygous	117392263
9	95298086	95298087	A	G	18	GENIC	homozygous	117392264
9	95298115	95298116	G	A	19	GENIC	homozygous	117392266
9	95298157	95298158	G	C	20	GENIC	homozygous	117392268
9	95298171	95298172	C	T	19	GENIC	homozygous	117392270
9	95298823	95298824	T	C	16	GENIC	homozygous	117392272
9	95299726	95299727	C	A	20	GENIC	homozygous	117602915
9	95300735	95300736	A	T	49	GENIC	homozygous	117602917
9	95302314	95302315	A	T	10	GENIC	homozygous	117392278