chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	34925243	34925244	A	G	38	GENIC	homozygous	110886882
2	34925384	34925385	T	C	38	GENIC	homozygous	109690485
2	34926153	34926154	T	G	24	GENIC	homozygous	110886883
2	34926751	34926752	G	T	22	GENIC	homozygous	110886884
2	34927365	34927366	A	C	24	GENIC	homozygous	110886885
2	34927860	34927861	G	A	10	GENIC	homozygous	110886886
2	34928498	34928499	G	C	19	GENIC	homozygous	110886887
2	34928752	34928753	A	G	9	GENIC	homozygous	110886888
2	34930142	34930143	C	A	30	GENIC	homozygous	110886889
2	34930320	34930321	G	A	25	GENIC	homozygous	110886890
2	34930685	34930686	A	G	21	GENIC	homozygous	109690489
2	34931599	34931600	G	T	19	GENIC	homozygous	109690491
2	34931768	34931769	A	G	24	GENIC	homozygous	109690493
2	34934305	34934306	C	T	55	GENIC	heterozygous	110886891
2	34934345	34934346	G	A	20	GENIC	homozygous	109690495
2	34934802	34934803	G	A	21	GENIC	homozygous	109690497
2	34934920	34934921	G	A	26	GENIC	homozygous	109690499
2	34937680	34937681	T	C	31	GENIC	homozygous	109690501
2	34938643	34938644	G	A	30	GENIC	homozygous	109690503
2	34938665	34938666	C	T	32	GENIC	homozygous	109690505
2	34938951	34938952	G	A	35	GENIC	homozygous	109690507
2	34940282	34940283	T	C	27	GENIC	homozygous	109690511