chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	131415136	131415137	T	C	21	GENIC	homozygous	137622926
5	131415442	131415443	G	A	26	GENIC	homozygous	143960626
5	131415458	131415458		G	27	GENIC	homozygous	137342141
5	131415460	131415462	CA		28	GENIC	homozygous	137342142
5	131416339	131416340	T	G	18	GENIC	homozygous	137622929
5	131417992	131417993	T	C	18	GENIC	homozygous	143960627
5	131418041	131418042	G	C	17	GENIC	homozygous	137622931
5	131418692	131418693	G	A	22	GENIC	homozygous	143960628
5	131418808	131418809	A	G	4	GENIC	heterozygous	137622933
5	131419456	131419457	T	A	20	GENIC	homozygous	137622934
5	131421064	131421065	C	T	30	GENIC	homozygous	143960629
5	131421490	131421491	A	T	16	GENIC	homozygous	143960630
5	131422478	131422479	A	T	16	GENIC	homozygous	143960631
5	131422550	131422551	A	C	8	GENIC	homozygous	143960632
5	131418870	131418871	T		12	GENIC	heterozygous	403158139
5	131418870	131418871	T	A	12	GENIC	possibly homozygous	154337126