chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13091642	13091643	A	G	49	GENIC	homozygous	115259742
12	13092357	13092358	T		34	GENIC	possibly homozygous	128961261
12	13092512	13092513	G	A	25	GENIC	homozygous	115259746
12	13096700	13096701	G	A	49	GENIC	homozygous	115259750
12	13097638	13097638		C	59	GENIC	homozygous	128961262
12	13098210	13098211	G	C	55	GENIC	homozygous	115259752
12	13102473	13102474	T	C	48	GENIC	homozygous	115259756
12	13103676	13103677	C	T	55	GENIC	homozygous	115259758
12	13103844	13103845	A	T	61	GENIC	homozygous	115259760
12	13104281	13104282	G	A	54	GENIC	homozygous	115259762
12	13105295	13105295		T	58	GENIC	homozygous	128961264
12	13093250	13093251	G	A	57	GENIC	homozygous	115416641
12	13098484	13098485	A	C	57	GENIC	homozygous	115416643
12	13105348	13105349	C	T	60	GENIC	homozygous	115416645
12	13094966	13094970	TGTA		14	GENIC	homozygous	132165522
12	13094936	13094936		TATTATTTTTTTAA	20	GENIC	heterozygous	132338079
12	13106259	13106259		CTGGAACTCAAAGTTTACC	54	GENIC	homozygous	128961265
12	13107182	13107183	C	T	54	GENIC	homozygous	115259768
12	13109211	13109212	C	T	63	GENIC	homozygous	115259772
12	13109316	13109317	G	A	46	GENIC	homozygous	115259774
12	13110695	13110696	T	C	61	GENIC	homozygous	115259776
12	13111748	13111749	A	G	58	GENIC	homozygous	115416647