chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	13091642	13091643	A	G	26	GENIC	homozygous	115259742
12	13092357	13092358	T		13	GENIC	homozygous	128961261
12	13092512	13092513	G	A	24	GENIC	homozygous	115259746
12	13093250	13093251	G	A	16	GENIC	homozygous	115416641
12	13094966	13094970	TGTA		5	GENIC	homozygous	132165522
12	13096700	13096701	G	A	17	GENIC	homozygous	115259750
12	13097638	13097638		C	20	GENIC	homozygous	128961262
12	13105295	13105295		T	16	GENIC	homozygous	128961264
12	13105348	13105349	C	T	24	GENIC	homozygous	115416645
12	13098210	13098211	G	C	22	GENIC	homozygous	115259752
12	13098484	13098485	A	C	25	GENIC	homozygous	115416643
12	13102473	13102474	T	C	17	GENIC	homozygous	115259756
12	13103676	13103677	C	T	16	GENIC	homozygous	115259758
12	13103844	13103845	A	T	15	GENIC	homozygous	115259760
12	13104281	13104282	G	A	22	GENIC	homozygous	115259762
12	13106259	13106259		CTGGAACTCAAAGTTTACC	14	GENIC	homozygous	128961265
12	13107182	13107183	C	T	23	GENIC	homozygous	115259768
12	13109211	13109212	C	T	17	GENIC	homozygous	115259772
12	13109316	13109317	G	A	12	GENIC	homozygous	115259774
12	13110695	13110696	T	C	27	GENIC	homozygous	115259776
12	13111748	13111749	A	G	16	GENIC	homozygous	115416647