chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	112069232	112069233	T	C	22	GENIC	homozygous	112006407
3	112071296	112071297	C	T	19	GENIC	homozygous	111675326
3	112071341	112071342	A	G	20	GENIC	homozygous	111675327
3	112071349	112071350	A	C	20	GENIC	homozygous	111675328
3	112073929	112073930	C	G	23	GENIC	homozygous	111675330
3	112074048	112074049	C	T	18	GENIC	homozygous	111675331
3	112074491	112074492	A	T	17	GENIC	homozygous	112006409
3	112074515	112074516	G	A	15	GENIC	homozygous	112006411
3	112075672	112075673	G	A	31	GENIC	homozygous	112006413
3	112076249	112076250	A	G	17	GENIC	homozygous	111675333
3	112080486	112080486		T	14	GENIC	homozygous	127918794
3	112080487	112080487		TT	15	GENIC	homozygous	127918795
3	112080488	112080488		TGTCATAACCTCTTTGTTAT	17	GENIC	homozygous	127918796
3	112080950	112080951	G	C	13	GENIC	homozygous	112006415
3	112081376	112081377	A	G	14	GENIC	homozygous	112006417
3	112081627	112081628	T	C	25	GENIC	homozygous	111675336
3	112082292	112082292		TTTTTTTC	10	GENIC	homozygous	127918797
3	112082946	112082947	G	A	12	GENIC	homozygous	111675338
3	112082000	112082001	C	T	12	GENIC	homozygous	112349918
3	112082854	112082860	ACACGC		13	GENIC	homozygous	130908141
3	112082945	112082945		CA	12	GENIC	homozygous	130908142