chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	103300578	103300579	C	T	28	GENIC	homozygous	109420284
1	103305648	103305649	C	T	18	GENIC	homozygous	109116668
1	103307196	103307197	A	G	17	GENIC	homozygous	109116686
1	103308678	103308679	G	A	13	GENIC	homozygous	109420290
1	103308758	103308759	A	C	21	GENIC	homozygous	109116700
1	103308937	103308938	C	T	27	GENIC	homozygous	109420292
1	103309191	103309192	C	T	14	GENIC	homozygous	109420294
1	103309901	103309902	C	T	17	GENIC	homozygous	109420296
1	103311085	103311086	G	A	15	GENIC	possibly homozygous	109420298
1	103311109	103311110	C	T	15	GENIC	homozygous	109116708
1	103311176	103311177	G	T	15	GENIC	homozygous	109420300
1	103311719	103311720	A	T	18	GENIC	homozygous	108165384
1	103311942	103311943	A	G	26	GENIC	homozygous	109116718
1	103312358	103312359	G	A	23	GENIC	homozygous	109420302
1	103313126	103313127	G	A	20	GENIC	homozygous	109420304
1	103313600	103313601	G	A	18	GENIC	homozygous	109116734
1	103313813	103313814	C	T	18	GENIC	homozygous	109116739
1	103313993	103313994	C	T	26	GENIC	homozygous	109420306
1	103315867	103315868	T	G	12	GENIC	homozygous	109116757
1	103316063	103316064	G	A	9	GENIC	homozygous	109420308
1	103320973	103320974	T	C	18	GENIC	homozygous	109116770
1	103321069	103321070	A	G	15	GENIC	homozygous	109116772
1	103321105	103321106	G	A	15	GENIC	homozygous	109420315
1	103321455	103321456	C	T	23	GENIC	homozygous	108903064
1	103321464	103321465	G	A	23	GENIC	homozygous	109116774
1	103321665	103321666	C	T	18	GENIC	homozygous	108903065
1	103321752	103321753	G	A	14	GENIC	homozygous	109116776
1	103322494	103322495	A	G	8	GENIC	homozygous	108903066
1	103322525	103322526	A	G	8	GENIC	homozygous	108903067
1	103322937	103322938	G	A	17	GENIC	homozygous	109420317
1	103323300	103323301	A	C	28	GENIC	homozygous	109116778