chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	740823	740824	C	G	19	GENIC	homozygous	109757962
19	741629	741630	T	C	19	GENIC	homozygous	109757964
19	742987	742988	C	T	34	GENIC	homozygous	109757966
19	743066	743067	A	G	28	GENIC	homozygous	109757968
19	743504	743505	C	T	34	GENIC	homozygous	109757970
19	743887	743888	C	G	34	GENIC	homozygous	109757972
19	745435	745436	G	A	32	GENIC	homozygous	109757974
19	745981	745982	A	C	30	GENIC	homozygous	109757976
19	746595	746596	T	C	22	GENIC	homozygous	109798966
19	747341	747342	C	A	22	GENIC	homozygous	109757981
19	747956	747957	C	G	21	GENIC	homozygous	109757983
19	749012	749013	G	A	33	GENIC	homozygous	109757987
19	749236	749237	A	G	26	GENIC	homozygous	109757989
19	751707	751708	G	A	23	GENIC	homozygous	109757992
19	752016	752017	A	T	18	GENIC	homozygous	109757994
19	752589	752590	A	C	27	GENIC	homozygous	109757996
19	753833	753834	A	G	28	GENIC	homozygous	109757998
19	753900	753901	T	C	29	GENIC	homozygous	109758000
19	755086	755087	A	C	22	GENIC	homozygous	109758002
19	755561	755562	C	T	30	GENIC	homozygous	109758004
19	756731	756732	C	T	28	GENIC	homozygous	109758006
19	758004	758005	G	T	34	GENIC	homozygous	109758008
19	759323	759324	T	C	25	GENIC	homozygous	109758010
19	759330	759331	T	A	28	GENIC	homozygous	109758012
19	759393	759394	A	C	33	GENIC	homozygous	109758014
19	759450	759451	T	G	30	GENIC	homozygous	109758016
19	759461	759462	T	G	30	GENIC	homozygous	109758019
19	759744	759745	T	G	23	GENIC	homozygous	109758021