chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101452385	101452386	G	A	42	GENIC	possibly homozygous	115018379
13	101476683	101476684	T	A	52	GENIC	heterozygous	118549908
13	101533337	101533338	G	A	29	GENIC	possibly homozygous	118467538
13	101551924	101551925	A	G	94	GENIC	heterozygous	118467539
13	101551952	101551953	G	A	53	GENIC	heterozygous	118467540
13	101551961	101551962	G	A	59	GENIC	heterozygous	118467541
13	101551976	101551977	C	T	84	GENIC	heterozygous	118467542
13	101552078	101552079	G	C	111	GENIC	heterozygous	118467543
13	101552140	101552141	A	G	94	GENIC	heterozygous	118506063
13	101552155	101552156	C	T	72	GENIC	heterozygous	118467544
13	101552212	101552213	G	A	64	GENIC	heterozygous	118506064
13	101552319	101552320	A	G	96	GENIC	heterozygous	118467545
13	101552347	101552348	G	A	61	GENIC	heterozygous	118467546
13	101552525	101552526	G	A	64	GENIC	heterozygous	118467547
13	101552604	101552605	G	A	154	GENIC	heterozygous	118467549
13	101552639	101552640	A	G	72	GENIC	heterozygous	118467550
13	101519892	101519893	C	G	34	GENIC	homozygous	114793101
13	101544316	101544317	C	T	18	GENIC	homozygous	114793103
13	101519893	101519894	A	G	35	GENIC	homozygous	114437811
13	101551899	101551900	C	G	143	GENIC	heterozygous	118570201
13	101552048	101552049	C	T	103	GENIC	heterozygous	118570203
13	101558029	101558030	A	T	51	GENIC	heterozygous	118570205
13	101558064	101558065	C	T	56	GENIC	heterozygous	118570207
13	101558338	101558339	C	T	130	GENIC	heterozygous	118570209
13	101574131	101574132	T	A	29	GENIC	homozygous	114437815
13	101574136	101574137	G	T	30	GENIC	homozygous	114437817
13	101584334	101584335	C	G	26	GENIC	homozygous	114585547
13	101596643	101596644	C	A	39	GENIC	homozygous	114437821
13	101596679	101596680	C	T	38	GENIC	homozygous	114437823
13	101596685	101596686	C	A	35	GENIC	homozygous	114437825
13	101596714	101596715	C	T	42	GENIC	homozygous	114437827