chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	129522048	129522049	G	T	34	GENIC	homozygous	113159928
4	129522737	129522738	T	C	43	GENIC	homozygous	113159929
4	129523885	129523886	G	A	36	GENIC	homozygous	113159930
4	129525388	129525389	A	G	42	GENIC	homozygous	113159931
4	129526913	129526914	C	T	43	GENIC	homozygous	113159932
4	129527878	129527879	A	G	44	GENIC	homozygous	113159933
4	129528551	129528552	A	G	42	GENIC	homozygous	113159934
4	129529851	129529852	G	A	39	GENIC	homozygous	113159935
4	129531379	129531380	G	T	39	GENIC	homozygous	113159936
4	129532671	129532672	C	T	48	GENIC	homozygous	113159937
4	129534149	129534150	A	G	45	GENIC	homozygous	113159938
4	129535359	129535359		GCTTCCTGGTTGCTGCCGCTGCAGAGAGCCCCTGGGCAGCACCCCACG	16	GENIC	heterozygous	132605321
4	129525362	129525363	T		40	GENIC	homozygous	132605319
4	129535094	129535094		GGG	9	GENIC	homozygous	132605320
4	129535985	129535994	TCCTGCTCC		33	GENIC	homozygous	131641863
4	129536092	129536093	C	A	40	GENIC	homozygous	113159939
4	129538377	129538377		TAT	42	GENIC	homozygous	131641865
4	129538584	129538585	G	A	51	GENIC	homozygous	113159940
4	129539099	129539100	G		21	GENIC	homozygous	131641866
4	129540506	129540507	C	T	47	GENIC	homozygous	113159941
4	129540855	129540856	T	C	46	GENIC	homozygous	113159942