chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	21225715	21225716	A	G	20	GENIC	homozygous	50286531
12	21225902	21225903	C	T	19	GENIC	possibly homozygous	50286532
12	21226078	21226079	G	A	11	GENIC	possibly homozygous	50286533
12	21226426	21226427	G	A	17	GENIC	homozygous	50286534
12	21226721	21226722	T	A	14	GENIC	homozygous	50286536
12	21227249	21227250	G	A	3	GENIC	homozygous	50286539
12	21228068	21228069	T	C	4	GENIC	homozygous	50286546
12	21228745	21228746	A	G	7	GENIC	homozygous	50286549
12	21229317	21229318	C	T	24	GENIC	possibly homozygous	50286551
12	21229559	21229560	A	G	7	GENIC	possibly homozygous	50286552
12	21229567	21229568	T	C	9	GENIC	homozygous	50286553
12	21231330	21231331	G	C	7	GENIC	heterozygous	50108491
12	21231331	21231332	G	T	7	GENIC	heterozygous	50108493
12	21231332	21231333	G	T	7	GENIC	heterozygous	50108495
12	21231747	21231748	T	A	17	GENIC	homozygous	50286558
12	21231800	21231801	G	A	15	GENIC	possibly homozygous	50286559
12	21231817	21231818	G	A	7	GENIC	homozygous	50286560
12	21232918	21232919	C	CTCTGTGTGTGTGCGTGGGTGTGGGTG	3	GENIC	heterozygous	50537622
12	21233109	21233110	C	T	17	GENIC	homozygous	50286571
12	21233822	21233823	A	G	14	GENIC	homozygous	50286572
12	21234499	21234500	T	A	14	GENIC	homozygous	50286587
12	21234587	21234588	G	-	5	GENIC	heterozygous	50286589
12	21235853	21235854	T	TAG	9	GENIC	homozygous	50286595
12	21235905	21235906	T	C	13	GENIC	homozygous	50286596
12	21235968	21235969	C	T	8	GENIC	homozygous	50286597