chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	907487	907488	C	CGTGT	17	GENIC	heterozygous	46041908
19	907622	907623	G	A	19	GENIC	homozygous	46041910
19	909386	909387	G	GTT	13	GENIC	homozygous	46041912
19	909980	909981	C	T	36	GENIC	homozygous	46041914
19	910392	910393	C	T	19	GENIC	homozygous	46041916
19	910886	910887	C	T	36	GENIC	homozygous	46041918
19	911263	911264	T	A	27	GENIC	homozygous	46041920
19	911378	911379	G	A	30	GENIC	homozygous	46041922
19	911762	911763	T	C	16	GENIC	homozygous	46041926
19	912112	912113	A	G	29	GENIC	homozygous	46041928
19	912144	912145	C	T	27	GENIC	homozygous	46041930
19	912147	912148	C	T	27	GENIC	homozygous	46041932
19	912399	912400	T	TGAGA	13	GENIC	homozygous	46041934
19	912430	912431	C	CTTTGTTTTGT	4	GENIC	homozygous	46041936
19	912619	912620	G	T	18	GENIC	homozygous	46041940
19	912678	912679	C	T	18	GENIC	homozygous	46041942
19	912757	912758	T	C	23	GENIC	homozygous	46041944
19	912875	912876	A	AGGG	11	GENIC	homozygous	46041946
19	913311	913312	G	A	30	GENIC	homozygous	46041952
19	913411	913412	T	C	31	GENIC	homozygous	46041954
19	913537	913538	T	C	19	GENIC	homozygous	46041956
19	913823	913824	C	G	29	GENIC	homozygous	46041958
19	913962	913963	A	G	31	GENIC	homozygous	46041960
19	914021	914022	G	A	23	GENIC	homozygous	46041962
19	914129	914130	T	C	23	GENIC	homozygous	46041964
19	914199	914200	T	C	13	GENIC	homozygous	46041966
19	914235	914236	T	C	12	GENIC	homozygous	46041968
19	914609	914610	G	A	26	GENIC	homozygous	46041970
19	914916	914918	GT	--	2	GENIC	homozygous	46041972
19	915033	915034	C	G	15	GENIC	homozygous	46041974
19	915148	915149	T	C	31	GENIC	homozygous	46041976
19	915229	915230	A	AAAAC	16	GENIC	homozygous	46041978
19	915341	915342	C	G	14	GENIC	homozygous	46041980
19	915408	915409	C	CT	8	GENIC	homozygous	46041982
19	915540	915541	G	C	26	GENIC	homozygous	46041984