chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	36059419	36059420	G	A	59	GENIC	possibly homozygous	46106636
19	36059979	36059980	A	G	38	GENIC	homozygous	46106638
19	36059997	36059998	A	G	47	GENIC	homozygous	46106640
19	36060167	36060168	A	G	36	GENIC	possibly homozygous	46106642
19	36060225	36060226	G	GA	35	GENIC	possibly homozygous	46106644
19	36060226	36060227	A	-	35	GENIC	heterozygous	46209839
19	36060803	36060804	A	-	5	GENIC	homozygous	46106646
19	36063938	36063939	A	AAAT	2	GENIC	homozygous	46209840
19	36066426	36066427	G	C	68	GENIC	homozygous	46106648
19	36067143	36067144	C	T	35	GENIC	possibly homozygous	46106650
19	36067489	36067491	AA	--	30	GENIC	heterozygous	46106652
19	36067490	36067491	A	-	30	GENIC	heterozygous	46209841
19	36067764	36067765	T	C	44	GENIC	possibly homozygous	46106654
19	36069123	36069124	T	A	46	GENIC	possibly homozygous	46106656
19	36069163	36069165	CC	--	9	GENIC	heterozygous	46209842
19	36069396	36069397	G	C	36	GENIC	homozygous	46106658
19	36069401	36069402	G	-	28	GENIC	homozygous	46106660
19	36069411	36069412	C	-	28	GENIC	homozygous	46106662
19	36069418	36069419	G	C	33	GENIC	possibly homozygous	46106664
19	36069421	36069422	A	-	28	GENIC	homozygous	46106666
19	36069426	36069427	A	T	32	GENIC	homozygous	46106668
19	36070443	36070444	G	T	65	GENIC	possibly homozygous	46106670