chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	1214224	1214225	C	A	4	GENIC	homozygous	116382442
7	1214330	1214331	A	T	24	GENIC	homozygous	115533133
7	1214908	1214909	A	G	30	GENIC	homozygous	115533135
7	1214913	1214914	A	T	33	GENIC	homozygous	115533136
7	1214966	1214967	G	T	41	GENIC	possibly homozygous	115533138
7	1215788	1215789	T	G	48	GENIC	homozygous	115533139
7	1215835	1215836	C	A	37	GENIC	homozygous	115533140
7	1226453	1226454	G	A	74	GENIC	heterozygous	115533150
7	1226464	1226465	G	A	72	GENIC	heterozygous	115533151
7	1226472	1226473	C	A	64	GENIC	heterozygous	115533152
7	1226498	1226499	C	A	61	GENIC	heterozygous	115973297
7	1226506	1226507	A	T	59	GENIC	heterozygous	116382443
7	1226518	1226519	A	G	63	GENIC	heterozygous	115973301
7	1235173	1235174	T	A	43	GENIC	heterozygous	115973313
7	1235251	1235252	C	T	52	GENIC	heterozygous	115973317
7	1235265	1235266	C	T	51	GENIC	heterozygous	115973319
7	1252762	1252763	C	A	29	GENIC	possibly homozygous	115973323
7	1262643	1262644	G	C	22	GENIC	heterozygous	115533167
7	1284438	1284439	C	G	18	GENIC	possibly homozygous	115533173