chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	111013932	111013933	C	G	55	GENIC	possibly homozygous	111673678
3	111014203	111014204	T	A	38	GENIC	homozygous	112139082
3	111014414	111014415	C	T	12	GENIC	homozygous	112139083
3	111014657	111014658	T	C	41	GENIC	homozygous	111673680
3	111016810	111016811	C	T	58	GENIC	homozygous	112139084
3	111017073	111017074	A	G	56	GENIC	possibly homozygous	111673682
3	111017173	111017174	T	C	47	GENIC	homozygous	112139085
3	111017586	111017587	A	G	42	GENIC	heterozygous	112139086
3	111017603	111017604	G	A	46	GENIC	heterozygous	112139087
3	111017673	111017674	A	G	43	GENIC	homozygous	112139088
3	111017800	111017801	C	T	59	GENIC	homozygous	112139089
3	111018593	111018594	T	C	52	GENIC	homozygous	112139090
3	111019133	111019134	G	A	34	GENIC	heterozygous	112139091
3	111019603	111019604	T	G	38	GENIC	homozygous	112139092
3	111020013	111020014	C	T	57	GENIC	homozygous	112139093
3	111020647	111020648	A	G	57	GENIC	homozygous	112139094
3	111021557	111021558	A	G	56	GENIC	homozygous	111673687