chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	48392249	48392250	G	GC	15	GENIC	possibly homozygous	46151081
19	48392844	48392845	C	-	1	GENIC	homozygous	46565665
19	48392858	48392859	C	CA	3	GENIC	homozygous	46565667
19	48394183	48394184	T	C	22	GENIC	homozygous	46151082
19	48394563	48394564	A	G	31	GENIC	homozygous	46151084
19	48397724	48397725	C	T	35	GENIC	homozygous	46151090
19	48398322	48398336	AAAAAAAAAAAAAA	--------------	14	GENIC	heterozygous	46151092
19	48398827	48398828	T	TAA	23	GENIC	homozygous	46151094
19	48399499	48399504	GGTTC	-----	19	GENIC	heterozygous	46445977
19	48399874	48399875	G	GTGTTGTTGT	11	GENIC	homozygous	46151095
19	48400978	48400980	TC	--	4	GENIC	homozygous	46565671
19	48400985	48400986	A	ATCT	4	GENIC	homozygous	46151098
19	48401054	48401055	T	-	14	GENIC	homozygous	46151099
19	48401843	48401844	T	C	30	GENIC	homozygous	46151101
19	48403409	48403410	T	TA	13	GENIC	homozygous	46151102
19	48403531	48403532	A	G	26	GENIC	homozygous	46151103
19	48404114	48404115	G	A	30	GENIC	homozygous	46151105
19	48404275	48404276	G	A	18	GENIC	homozygous	46151106
19	48404324	48404325	C	CGTGT	7	GENIC	possibly homozygous	46565673
19	48405657	48405658	G	GT	23	GENIC	homozygous	46151111