chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	51351425	51351426	T	C	30	GENIC	homozygous	50244509
12	51351890	51351891	C	T	18	GENIC	homozygous	50244511
12	51352716	51352717	A	G	21	GENIC	possibly homozygous	50472563
12	51353195	51353196	T	C	40	GENIC	homozygous	50244513
12	51353730	51353731	T	C	25	GENIC	homozygous	50244515
12	51354051	51354052	T	C	24	GENIC	homozygous	50244517
12	51354655	51354656	A	C	27	GENIC	homozygous	50244519
12	51354913	51354914	T	A	28	GENIC	homozygous	50244521
12	51355536	51355537	A	T	22	GENIC	homozygous	50244523
12	51355550	51355551	A	T	21	GENIC	homozygous	50244525
12	51355573	51355574	T	G	20	GENIC	homozygous	50244527
12	51355770	51355771	A	-	15	GENIC	homozygous	50472564
12	51355923	51355924	G	-	19	GENIC	homozygous	50244531
12	51356274	51356275	G	A	24	GENIC	homozygous	50244533
12	51356406	51356407	C	T	27	GENIC	homozygous	50244535
12	51356751	51356752	T	C	22	GENIC	homozygous	50244537
12	51356935	51356936	T	C	27	GENIC	homozygous	50244539
12	51357919	51357920	C	A	30	GENIC	homozygous	50244541
12	51358656	51358658	CT	--	46	GENIC	homozygous	50244543
12	51358759	51358760	C	A	34	GENIC	possibly homozygous	50244545
12	51359633	51359634	A	AG	26	GENIC	homozygous	50244547
12	51359793	51359794	C	G	21	GENIC	homozygous	50472565
12	51359992	51359993	C	T	29	GENIC	possibly homozygous	50244555
12	51360248	51360249	T	C	24	GENIC	homozygous	50244557
12	51360398	51360399	A	G	23	GENIC	homozygous	50244559
12	51360530	51360531	C	CCAGG	20	GENIC	homozygous	50244561
12	51360566	51360567	G	A	27	GENIC	homozygous	50244563
12	51360568	51360569	C	T	28	GENIC	homozygous	50244565
12	51360909	51360910	C	A	30	GENIC	homozygous	50244567
12	51361061	51361062	G	A	17	GENIC	homozygous	50244569
12	51361289	51361290	A	G	23	GENIC	homozygous	50244571