chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	14073789	14073790	G	C	32	GENIC	heterozygous	112511456
4	14073793	14073794	A	T	30	GENIC	heterozygous	112511458
4	14073797	14073798	A	G	35	GENIC	heterozygous	112511460
4	14073807	14073808	G	A	41	GENIC	possibly homozygous	112511462
4	14073811	14073812	G	C	45	GENIC	possibly homozygous	112511464
4	14073866	14073867	G	A	68	GENIC	possibly homozygous	112511466
4	14073872	14073873	A	C	66	GENIC	possibly homozygous	112511468
4	14073882	14073883	A	G	69	GENIC	possibly homozygous	112511470
4	14073908	14073909	C	A	52	GENIC	heterozygous	112511472
4	14073957	14073958	A	G	32	GENIC	heterozygous	112511474
4	14076312	14076313	G	A	94	GENIC	heterozygous	112511476
4	14076377	14076378	C	T	75	GENIC	homozygous	112511478
4	14076457	14076458	C	T	16	GENIC	heterozygous	112998165
4	14096546	14096547	T	A	4	GENIC	homozygous	112998166
4	14096553	14096554	A	T	7	GENIC	homozygous	112998167
4	14096608	14096609	T	C	29	GENIC	homozygous	112511480
4	14097201	14097202	G	A	25	GENIC	possibly homozygous	112511482
4	14097202	14097203	T	C	25	GENIC	possibly homozygous	112511484
4	14102331	14102332	G	A	67	GENIC	homozygous	112511485
4	14109403	14109404	G	A	120	GENIC	homozygous	112511487
4	14109426	14109427	T	C	130	GENIC	homozygous	112511488
4	14109770	14109771	A	G	78	GENIC	heterozygous	112511490
4	14110528	14110529	T	A	43	GENIC	heterozygous	112998168
4	14110541	14110542	G	A	49	GENIC	heterozygous	112511492
4	14110579	14110580	A	T	57	GENIC	homozygous	112511494
4	14110586	14110587	A	G	56	GENIC	homozygous	112511496
4	14110738	14110739	A	T	61	GENIC	homozygous	112511498