chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	104799947	104799948	C		7	GENIC	heterozygous	403014594
2	104799947	104799948	C	T	7	GENIC	homozygous	403014595
2	104835058	104835059	A	G	66	GENIC	heterozygous	140979899
2	104898710	104898711	A	T	24	GENIC	heterozygous	146361840
2	104898710	104898711	A		24	GENIC	heterozygous	403014610
2	104917073	104917074	G	C	46	GENIC	homozygous	136244324
2	104917080	104917081	T	G	43	GENIC	homozygous	403014615
2	104917080	104917081	T		43	GENIC	heterozygous	403014616
2	104917083	104917084	T	G	40	GENIC	homozygous	403014617
2	104917083	104917084	T		40	GENIC	heterozygous	403014618
2	104917086	104917087	C	G	38	GENIC	homozygous	403014619
2	104917086	104917087	C	T	38	GENIC	heterozygous	403014620
2	104917086	104917087	C		38	GENIC	heterozygous	403014621
2	104917089	104917090	T	G	39	GENIC	possibly homozygous	136244325
2	104917100	104917101	T	G	34	GENIC	possibly homozygous	136244326
2	104917125	104917126	T	G	31	GENIC	possibly homozygous	140979900