chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48980577	48980578	C	CG	2	GENIC	homozygous	50230540
12	48982997	48982998	A	C	2	GENIC	homozygous	50230548
12	48983376	48983377	A	G	10	GENIC	homozygous	50230552
12	48983620	48983621	T	TC	6	GENIC	homozygous	50230554
12	48983866	48983867	G	A	16	GENIC	possibly homozygous	50230556
12	48984374	48984375	C	T	18	GENIC	homozygous	50230558
12	48985532	48985533	G	A	6	GENIC	heterozygous	50230560
12	48985647	48985648	A	ATG	16	GENIC	possibly homozygous	50230562
12	48985698	48985699	T	C	26	GENIC	homozygous	50230564
12	48985974	48985975	A	G	20	GENIC	possibly homozygous	50230566
12	48986053	48986054	A	C	21	GENIC	possibly homozygous	50230568
12	48986166	48986167	A	G	27	GENIC	possibly homozygous	50230570
12	48986527	48986528	T	C	5	GENIC	heterozygous	50230574
12	48986808	48986809	G	GT	6	GENIC	homozygous	50230579
12	48987178	48987179	C	T	24	GENIC	possibly homozygous	50230581
12	48987259	48987260	C	T	11	GENIC	homozygous	50230583
12	48987287	48987288	A	G	11	GENIC	homozygous	50230585
12	48987293	48987294	A	G	10	GENIC	homozygous	50230587
12	48987767	48987768	C	G	14	GENIC	homozygous	50230589
12	48988842	48988843	C	A	18	GENIC	possibly homozygous	50230593
12	48989503	48989504	C	T	14	GENIC	homozygous	50230601
12	48989617	48989618	G	A	23	GENIC	possibly homozygous	50230603
12	48989742	48989743	A	AC	9	GENIC	possibly homozygous	50230605
12	48990289	48990290	T	C	16	GENIC	possibly homozygous	50230607
12	48990573	48990574	A	G	25	GENIC	homozygous	50230609
12	48990788	48990789	A	ATCAGTTGGGCGTGCTGATGGGCACGTACCTCTTCCAACG	2	GENIC	homozygous	50513686
12	48992385	48992386	A	G	15	GENIC	homozygous	50230611
12	48993260	48993261	C	G	25	GENIC	homozygous	50230613
12	48993621	48993622	T	C	23	GENIC	homozygous	50230615
12	48995586	48995587	A	G	4	GENIC	homozygous	50230621
12	48995595	48995596	T	A	9	GENIC	possibly homozygous	50230623
12	48996004	48996005	G	C	13	GENIC	possibly homozygous	50230624
12	48996796	48996797	A	G	6	GENIC	homozygous	50230626
12	48997498	48997499	G	T	21	GENIC	possibly homozygous	50230632
12	48997812	48997813	G	T	25	GENIC	homozygous	50230634
12	48998138	48998139	C	-	2	GENIC	homozygous	50230638
12	48998143	48998144	G	A	2	GENIC	homozygous	50230640
12	48998225	48998226	G	GT	8	GENIC	possibly homozygous	50230642
12	48998762	48998763	T	A	23	GENIC	possibly homozygous	50230644
12	49000112	49000113	T	C	12	GENIC	heterozygous	50230646
12	49000652	49000653	G	A	9	GENIC	homozygous	50230648
12	49000767	49000768	A	AAAAC	1	GENIC	homozygous	50230650
12	49000802	49000803	G	A	8	GENIC	heterozygous	50230652
12	49000994	49000995	T	C	16	GENIC	possibly homozygous	50230654
12	49001434	49001435	C	G	24	GENIC	homozygous	50230660
12	49001740	49001741	C	T	23	GENIC	possibly homozygous	50230662
12	49001795	49001796	A	G	15	GENIC	homozygous	50230664
12	49001807	49001808	C	T	17	GENIC	homozygous	50230666
12	49002189	49002190	T	C	22	GENIC	possibly homozygous	50230668
12	49002317	49002318	C	T	16	GENIC	possibly homozygous	50230670
12	49002761	49002765	TCTG	----	4	GENIC	homozygous	50230672
12	49002908	49002909	T	C	17	GENIC	possibly homozygous	50230674
12	49002978	49002979	T	C	14	GENIC	homozygous	50230676
12	49003778	49003779	C	T	15	GENIC	homozygous	50230685
12	49003807	49003809	TC	--	12	GENIC	heterozygous	50546588
12	49004250	49004251	T	G	10	GENIC	possibly homozygous	50230689
12	49004251	49004252	C	T	10	GENIC	possibly homozygous	50230691
12	49004305	49004306	T	A	15	GENIC	homozygous	50230693
12	49004381	49004382	C	G	15	GENIC	homozygous	50230695
12	49004862	49004863	T	TA	13	GENIC	homozygous	50230697
12	48989742	48989743	A	ACCC	9	GENIC	heterozygous	50593128