chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	137958021	137958021		C	41	GENIC	homozygous	127934851
3	137958033	137958033		C	43	GENIC	homozygous	127934852
3	137958052	137958053	G	A	41	GENIC	homozygous	119740568
3	137958052	137958052		C	41	GENIC	homozygous	127934853
3	137958058	137958058		C	42	GENIC	homozygous	127934854
3	137958072	137958072		G	37	GENIC	homozygous	127934855
3	137958076	137958077	C	A	38	GENIC	homozygous	119914725
3	137958078	137958079	A		38	GENIC	homozygous	127934856
3	137958089	137958090	C		35	GENIC	homozygous	127934857
3	137958103	137958107	ATGG		35	GENIC	homozygous	127934858
3	137958113	137958114	G		34	GENIC	homozygous	127934859
3	137958117	137958118	G		34	GENIC	homozygous	127934860
3	137958126	137958127	G		35	GENIC	homozygous	127934861
3	137960350	137960352	AC		30	GENIC	heterozygous	130283529
3	137966604	137966636	AGTGTCTATCCAGGTATCCATAAATGATGATA		12	GENIC	homozygous	130283530
3	137967113	137967113		T	44	GENIC	homozygous	127934882
3	137984274	137984275	T		41	GENIC	homozygous	127934888