chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	30968783	30968784	A	AGCCTCT	3	GENIC	homozygous	50510926
13	30968950	30968951	C	A	24	GENIC	homozygous	49702617
13	30970296	30970298	AC	--	17	GENIC	heterozygous	50548912
13	30972328	30972329	C	CGAT	18	GENIC	possibly homozygous	49702618
13	30977169	30977170	C	T	30	GENIC	homozygous	49702623
13	30977194	30977195	C	A	30	GENIC	homozygous	49702624
13	30977212	30977213	T	C	35	GENIC	homozygous	49702625
13	30977787	30977788	C	G	33	GENIC	homozygous	49702626
13	30977846	30977932	GGTCTCTCCAGAGTGACACGCCGTATCATCTGTGGGGTCTCTCCAGAGTGGCACGCTGTATCATCTGTGGGGTCTCTCCAGAGTCT	--------------------------------------------------------------------------------------	13	GENIC	heterozygous	50487713
13	30979125	30979127	AA	--	16	GENIC	homozygous	49702634
13	30979789	30979790	T	C	26	GENIC	homozygous	49702635
13	30980243	30980244	A	T	19	GENIC	homozygous	49702636
13	30980501	30980502	T	TATG	11	GENIC	homozygous	49702637
13	30980610	30980611	T	TTATTTATTTA	13	GENIC	heterozygous	50510928
13	30980698	30980699	T	G	16	GENIC	homozygous	49702638
13	30980880	30980881	T	C	20	GENIC	homozygous	49702639
13	30980957	30980958	A	G	18	GENIC	homozygous	49702640
13	30981393	30981394	C	A	50	GENIC	homozygous	49702641
13	30981532	30981533	C	T	31	GENIC	homozygous	49702642
13	30982330	30982331	G	A	12	GENIC	homozygous	49702643
13	30983506	30983507	A	AC	26	GENIC	homozygous	49702644
13	30984114	30984115	C	T	35	GENIC	homozygous	49702651
13	30984268	30984269	T	C	28	GENIC	homozygous	49702652
13	30984283	30984284	G	A	31	GENIC	homozygous	49702653
13	30984358	30984359	C	T	34	GENIC	homozygous	49702654
13	30984372	30984373	G	C	36	GENIC	homozygous	49702655
13	30984381	30984382	T	C	38	GENIC	homozygous	49702656
13	30984775	30984776	A	C	42	GENIC	homozygous	49702657
13	30986316	30986317	C	T	32	GENIC	homozygous	49702658
13	30986481	30986482	A	G	30	GENIC	homozygous	49702659
13	30986875	30986876	G	A	26	GENIC	homozygous	49702660
13	30986895	30986896	G	T	25	GENIC	homozygous	49702661
13	30987012	30987013	G	A	29	GENIC	homozygous	49702662
13	30987013	30987014	T	G	29	GENIC	homozygous	49702663
13	30987704	30987705	T	TTTA	4	GENIC	homozygous	49702664
13	30988419	30988420	G	T	31	GENIC	homozygous	50809119
13	30988609	30988610	C	T	34	GENIC	homozygous	49702666
13	30989437	30989438	G	A	36	GENIC	homozygous	49702667
13	30989913	30989914	G	A	34	GENIC	homozygous	49702668
13	30989925	30989926	G	-	33	GENIC	homozygous	49702669
13	30990355	30990356	T	A	36	GENIC	homozygous	49702670
13	30990359	30990360	G	A	38	GENIC	homozygous	49702671
13	30991110	30991111	C	G	22	GENIC	homozygous	49702672
13	30991249	30991250	C	T	16	GENIC	homozygous	49702673
13	30991321	30991322	C	CCA	17	GENIC	homozygous	49702674
13	30991502	30991503	C	-	3	GENIC	homozygous	49702675
13	30992159	30992160	G	A	35	GENIC	homozygous	49702677
13	30992237	30992238	C	T	32	GENIC	homozygous	49702678
13	30993032	30993033	A	AACACAC	16	GENIC	heterozygous	50510930
13	30993032	30993033	A	AACACACAC	16	GENIC	heterozygous	50510932
13	30994316	30994318	GA	--	3	GENIC	heterozygous	50510934
13	30995015	30995016	T	C	26	GENIC	homozygous	49702681
13	30995439	30995440	C	T	32	GENIC	homozygous	49702682
13	30997122	30997123	C	-	25	GENIC	homozygous	49702683
13	30997161	30997162	T	TC	22	GENIC	homozygous	49702684
13	30997434	30997435	C	A	20	GENIC	homozygous	49702685
13	30997661	30997662	T	TAAAGAAAGAATGAATAGGGGCTGGGGATTTAGCTCAGTGGTAGAGCGCTTACCTAGGAAGCGCAAGGCCCTGGGTTCGGTCCCCAGCTCCGAAAAAAAGAACAAAAAAAAAAAAAAAAAAA	39	GENIC	possibly homozygous	50510936