chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	94251929	94251930	G	C	45	GENIC	homozygous	141219218
1	94252115	94252116	A	G	39	GENIC	homozygous	141219219
1	94252444	94252445	C	T	42	GENIC	homozygous	141219220
1	94252625	94252625		GTGTGTGGAA	15	GENIC	homozygous	141163382
1	94252697	94252698	C	T	20	GENIC	homozygous	141219221
1	94253557	94253558	C		46	GENIC	homozygous	141163383
1	94253831	94253832	A	G	41	GENIC	homozygous	141219222
1	94254102	94254103	T	C	39	GENIC	homozygous	141219223
1	94255097	94255098	A	T	43	GENIC	homozygous	141219224
1	94255231	94255232	A	C	39	GENIC	homozygous	141219225
1	94255256	94255256		TTTG	23	GENIC	homozygous	141163384
1	94255268	94255269	A	T	27	GENIC	homozygous	141219226
1	94255275	94255275		GA	27	GENIC	homozygous	141163385
1	94255820	94255821	T	G	34	GENIC	homozygous	141219227
1	94255927	94255928	C	T	37	GENIC	homozygous	141219228
1	94256221	94256222	T	C	35	GENIC	homozygous	141219229
1	94256292	94256293	G	A	38	GENIC	homozygous	141219230
1	94256329	94256330	C		35	GENIC	homozygous	141163386
1	94256332	94256340	CCTCCTCC		35	GENIC	homozygous	141163387
1	94256380	94256381	C	T	30	GENIC	homozygous	141219231
1	94256521	94256522	C		27	GENIC	homozygous	141163388
1	94256789	94256790	A	G	40	GENIC	homozygous	141219232
1	94256934	94256935	A	G	54	GENIC	possibly homozygous	141219233
1	94258338	94258339	C	A	37	GENIC	homozygous	141219234
1	94258386	94258387	T	C	31	GENIC	homozygous	141219235