chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	114065876	114065877	T	C	23	GENIC	homozygous	112009769
3	114066048	114066049	G	T	18	GENIC	homozygous	112009771
3	114066110	114066111	T	C	16	GENIC	homozygous	112009773
3	114066145	114066146	C	T	16	GENIC	homozygous	112009774
3	114066997	114066998	T	C	14	GENIC	homozygous	112009776
3	114067607	114067608	A	G	17	GENIC	homozygous	111678180
3	114067908	114068016	AAAAACTTGCTATTGGGGGGAGGGGGATGTTTGCCCGGAAACCGGGAAAGGGAATAACACTCGAAATGTATATAAGAAATACTCAAGTTAATTAAAAAAAAAAAAAAA		12	GENIC	homozygous	133115900
3	114068151	114068151		TTT	19	GENIC	homozygous	133115901
3	114068524	114068525	T	A	10	GENIC	homozygous	112009778
3	114068571	114068572	G	A	22	GENIC	homozygous	112009780
3	114068606	114068606		A	26	GENIC	homozygous	133115902
3	114068707	114068708	A	G	29	GENIC	homozygous	112009782
3	114069304	114069305	T	C	19	GENIC	homozygous	112009784
3	114069587	114069588	T	C	17	GENIC	homozygous	112009786
3	114069981	114069982	T	C	16	GENIC	homozygous	111678182
3	114070351	114070352	C	G	20	GENIC	homozygous	112009788
3	114072872	114072876	GGGT		17	GENIC	homozygous	133115903
3	114072881	114072882	A	G	17	GENIC	homozygous	112009796
3	114070818	114070819	C	T	31	GENIC	homozygous	112009790
3	114071200	114071201	A	G	23	GENIC	homozygous	112009792
3	114071408	114071409	C	T	27	GENIC	homozygous	112009794
3	114073597	114073598	T	G	23	GENIC	homozygous	112009798
3	114073626	114073627	G	A	19	GENIC	homozygous	112009800
3	114074741	114074742	A	G	29	GENIC	possibly homozygous	111678184
3	114074850	114074851	A	G	17	GENIC	homozygous	112009802
3	114075024	114075025	C	T	30	GENIC	homozygous	112009804