chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	263913989	263913990	A	G	33	GENIC	homozygous	108634368
1	263914210	263914211	T	C	36	GENIC	homozygous	108634370
1	263914932	263914933	C	T	35	GENIC	homozygous	108634372
1	263917120	263917121	C	T	34	GENIC	heterozygous	109217550
1	263917124	263917125	T	C	36	GENIC	heterozygous	108634376
1	263917161	263917162	C	T	40	GENIC	possibly homozygous	108634378
1	263917246	263917247	A	G	33	GENIC	homozygous	108634381
1	263917407	263917408	A	C	50	GENIC	homozygous	108634383
1	263917534	263917535	A	C	25	GENIC	homozygous	108634385
1	263918066	263918067	G	A	40	GENIC	homozygous	108634387
1	263919098	263919099	T	C	15	GENIC	homozygous	108634388
1	263919732	263919733	G	A	33	GENIC	possibly homozygous	108634392
1	263919763	263919764	C	T	27	GENIC	homozygous	108634394
1	263919802	263919803	C	T	25	GENIC	homozygous	108634396
1	263919877	263919878	T	C	28	GENIC	homozygous	108634397
1	263920743	263920744	A	G	29	GENIC	homozygous	108634399
1	263920975	263920976	C	T	32	GENIC	homozygous	109217552