chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	142672307	142672308	A	T	22	GENIC	homozygous	110760104
2	142672322	142672323	C	G	28	GENIC	homozygous	110760105
2	142672448	142672449	T	A	18	GENIC	homozygous	110760106
2	142672511	142672512	C	A	18	GENIC	homozygous	110760107
2	142672598	142672599	G	A	23	GENIC	homozygous	110760108
2	142672823	142672824	C	T	22	GENIC	homozygous	110760109
2	142672950	142672951	C	T	32	GENIC	homozygous	110760110
2	142673000	142673001	C	G	33	GENIC	homozygous	110760111
2	142673163	142673164	G	A	31	GENIC	homozygous	110760112
2	142673422	142673423	C	T	31	GENIC	homozygous	110760113
2	142673519	142673520	G	C	45	GENIC	homozygous	110760114
2	142673605	142673606	C	T	31	GENIC	homozygous	110760115
2	142673612	142673613	T	C	35	GENIC	homozygous	110760116
2	142674804	142674805	G	A	17	GENIC	homozygous	110760117
2	142674849	142674850	T	C	20	GENIC	homozygous	110760118
2	142676125	142676126	G	A	23	GENIC	homozygous	110760119
2	142678880	142678881	G	A	29	GENIC	homozygous	110760120
2	142680533	142680534	A	T	6	GENIC	homozygous	110890452
2	142684976	142684977	A	T	17	GENIC	homozygous	110760121
2	142685264	142685265	C	T	22	GENIC	homozygous	110760122