chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52867490	52867491	G	GT	43	GENIC	homozygous	50361627
13	52867652	52867653	C	T	23	GENIC	homozygous	50361629
13	52868394	52868395	A	G	35	GENIC	homozygous	50361631
13	52868584	52868585	C	T	63	GENIC	homozygous	50361633
13	52868693	52868694	C	T	49	GENIC	homozygous	50361635
13	52868909	52868910	A	T	27	GENIC	homozygous	50361637
13	52869006	52869007	C	CCTAAACAGCCTAGCCCGTTAG	6	GENIC	homozygous	50361639
13	52869068	52869069	C	T	24	GENIC	possibly homozygous	49758375
13	52869070	52869071	C	-	23	GENIC	homozygous	49758376
13	52869553	52869554	A	C	32	GENIC	homozygous	50361641
13	52870177	52870178	G	A	31	GENIC	homozygous	50361643
13	52870225	52870226	G	A	23	GENIC	homozygous	50361645
13	52870283	52870284	G	C	34	GENIC	homozygous	50361647
13	52870322	52870323	T	C	38	GENIC	homozygous	50361649
13	52870437	52870438	A	G	46	GENIC	homozygous	50361651
13	52870638	52870643	AAAAA	-----	8	GENIC	homozygous	50361653
13	52872028	52872029	A	G	24	GENIC	homozygous	50361655
13	52879449	52879450	C	T	7	GENIC	homozygous	50361659
13	52894576	52894577	T	-	69	GENIC	homozygous	49758380
13	52895618	52895619	G	A	30	GENIC	possibly homozygous	49758381
13	52895620	52895621	T	A	32	GENIC	homozygous	49758382
13	52912191	52912192	C	T	15	GENIC	homozygous	50361661