chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	129708205	129708206	A	G	16	GENIC	homozygous	60023622
3	129708285	129708286	A	AG	25	GENIC	possibly homozygous	57670664
3	129708791	129708792	A	T	27	GENIC	homozygous	57670670
3	129708793	129708794	A	AGCTGTC	28	GENIC	homozygous	57670672
3	129708795	129708796	G	C	29	GENIC	homozygous	57670674
3	129708888	129708889	G	A	25	GENIC	homozygous	60023623
3	129709522	129709523	A	G	19	GENIC	homozygous	60023624
3	129709753	129709754	C	CGTGTGTGTGTGT	5	GENIC	homozygous	58809125
3	129709796	129709797	G	A	22	GENIC	homozygous	60023625
3	129709807	129709808	T	C	21	GENIC	homozygous	57670678
3	129709954	129709955	G	T	16	GENIC	homozygous	60023626
3	129711150	129711151	A	-	37	GENIC	homozygous	60023627
3	129711886	129711887	T	TCACA	1	GENIC	homozygous	58695713
3	129712146	129712147	T	G	30	GENIC	homozygous	57670692
3	129712681	129712682	C	CATGCCT	27	GENIC	homozygous	57670694
3	129712869	129712870	G	A	30	GENIC	homozygous	60023628
3	129713180	129713181	T	C	30	GENIC	homozygous	60023629
3	129714047	129714048	A	G	23	GENIC	homozygous	57670701
3	129714201	129714202	A	AT	21	GENIC	homozygous	60023630
3	129715054	129715055	G	A	27	GENIC	homozygous	57670709
3	129715270	129715271	A	G	26	GENIC	homozygous	57670713
3	129715333	129715334	T	TAG	27	GENIC	homozygous	57670715
3	129715599	129715600	G	A	25	GENIC	homozygous	57670719
3	129716465	129716466	C	CCTGCCT	17	GENIC	homozygous	57670721
3	129716492	129716497	TTTTT	-----	17	GENIC	homozygous	59422301
3	129716506	129716507	T	A	18	GENIC	possibly homozygous	60023631
3	129717341	129717342	C	T	37	GENIC	homozygous	60023632
3	129717983	129717984	T	G	26	GENIC	homozygous	60023633
3	129718668	129718669	T	TA	17	GENIC	possibly homozygous	60023634
3	129715219	129715220	C	-	8	GENIC	heterozygous	59292875