chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	200617182	200617183	G	C	42	GENIC	possibly homozygous	110204862
2	200617247	200617248	C	T	46	GENIC	possibly homozygous	110204863
2	200617253	200617254	C	A	48	GENIC	possibly homozygous	110204864
2	200624582	200624583	A	G	17	GENIC	possibly homozygous	110204869
2	200624635	200624636	G	A	43	GENIC	possibly homozygous	111356734
2	200624782	200624783	T	C	44	GENIC	homozygous	111356736
2	200624812	200624813	C	T	43	GENIC	homozygous	110204870
2	200624900	200624901	C	T	44	GENIC	homozygous	111356738
2	200626215	200626216	C	T	44	GENIC	possibly homozygous	111356740
2	200627081	200627082	G	A	38	GENIC	possibly homozygous	111356742
2	200627249	200627250	A	T	42	GENIC	homozygous	111356744
2	200628007	200628008	T	C	47	GENIC	homozygous	110204872
2	200628314	200628315	C	T	22	GENIC	homozygous	111356746
2	200629007	200629008	G	A	42	GENIC	possibly homozygous	110204877
2	200629139	200629140	T	C	42	GENIC	homozygous	111356748
2	200630724	200630725	G	A	39	GENIC	homozygous	111356750
2	200631247	200631248	C	T	14	GENIC	heterozygous	111356752
2	200631539	200631540	C	A	45	GENIC	homozygous	110204878
2	200632225	200632226	T	C	50	GENIC	possibly homozygous	110204880
2	200630569	200630570	A	C	49	GENIC	homozygous	111000456