chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	121728229	121728230	C	G	55	GENIC	possibly homozygous	111690011
3	121729643	121729644	G	C	38	GENIC	homozygous	111690012
3	121730387	121730388	T	G	44	GENIC	homozygous	111690013
3	121730795	121730796	T	G	31	GENIC	homozygous	111690015
3	121732028	121732029	C	A	34	GENIC	homozygous	111690016
3	121732341	121732342	T	C	44	GENIC	homozygous	111690017
3	121733322	121733324	TA		50	GENIC	homozygous	127924888
3	121730622	121730624	TA		36	GENIC	heterozygous	127924886
3	121732688	121732822	CCCCATGTCTGATTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTGGTTCTTTTTTTTTTTCCGGAGCTGGGGACCAAACCCAGGGCCTTGCGCTTCCTAGGCAAGCGCTCTACCACTGAGCTAAATCCCCAACCC		32	GENIC	homozygous	127924887
3	121737091	121737096	TCAGT		70	GENIC	homozygous	127924889