chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	52867490	52867491	G	GT	25	GENIC	homozygous	50361627
13	52867652	52867653	C	T	27	GENIC	homozygous	50361629
13	52868394	52868395	A	G	34	GENIC	homozygous	50361631
13	52868584	52868585	C	T	31	GENIC	homozygous	50361633
13	52868693	52868694	C	T	21	GENIC	homozygous	50361635
13	52868909	52868910	A	T	22	GENIC	homozygous	50361637
13	52869006	52869007	C	CCTAAACAGCCTAGCCCGTTAG	23	GENIC	homozygous	50361639
13	52869068	52869069	C	T	28	GENIC	homozygous	49758375
13	52869070	52869071	C	-	29	GENIC	homozygous	49758376
13	52869553	52869554	A	C	18	GENIC	homozygous	50361641
13	52870177	52870178	G	A	33	GENIC	homozygous	50361643
13	52870225	52870226	G	A	39	GENIC	homozygous	50361645
13	52870283	52870284	G	C	33	GENIC	homozygous	50361647
13	52870322	52870323	T	C	23	GENIC	homozygous	50361649
13	52870437	52870438	A	G	34	GENIC	homozygous	50361651
13	52870638	52870643	AAAAA	-----	5	GENIC	homozygous	50361653
13	52890033	52890034	C	CA	9	GENIC	homozygous	50518101
13	52894576	52894577	T	-	35	GENIC	homozygous	49758380
13	52896129	52896135	ACACAC	------	1	GENIC	homozygous	50563264