chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	123558579	123558580	T	C	44	GENIC	homozygous	110003994
2	123594537	123594538	C	A	113	GENIC	heterozygous	110003995
2	123602087	123602088	C	T	53	GENIC	heterozygous	110003996
2	123603796	123603797	T	A	30	GENIC	heterozygous	110003997
2	123603873	123603874	A	C	51	GENIC	heterozygous	110003998
2	123603901	123603902	C	T	43	GENIC	heterozygous	110003999
2	123603909	123603910	C	G	40	GENIC	heterozygous	110004000
2	123603918	123603919	C	T	36	GENIC	heterozygous	110004001
2	123603934	123603935	C	T	39	GENIC	heterozygous	110004002
2	123603938	123603939	C	G	38	GENIC	heterozygous	110004003
2	123626335	123626336	C	A	143	GENIC	heterozygous	110004004
2	123627345	123627346	A	T	39	GENIC	heterozygous	110004005
2	123653153	123653154	G	A	152	GENIC	heterozygous	110004006
2	123655129	123655130	A	C	22	GENIC	homozygous	110004007
2	123666424	123666425	G	T	19	GENIC	homozygous	110004008
2	123666998	123666999	A	T	80	GENIC	heterozygous	110004009
2	123669799	123669800	C	T	95	GENIC	heterozygous	110004010
2	123669809	123669810	G	T	89	GENIC	heterozygous	110004011
2	123669944	123669945	T	A	82	GENIC	heterozygous	110004012
2	123725483	123725484	C	A	144	GENIC	heterozygous	110004013
2	123728370	123728371	G	A	123	GENIC	heterozygous	110004014
2	123729351	123729352	T	C	152	GENIC	heterozygous	110004015
2	123741568	123741569	A	C	27	GENIC	homozygous	110004016