chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	112087343	112087344	C	G	11	GENIC	homozygous	112006423
3	112087568	112087569	G	T	21	GENIC	homozygous	112139313
3	112088525	112088526	G	A	18	GENIC	homozygous	112006425
3	112088594	112088595	T	C	19	GENIC	homozygous	112006427
3	112088829	112088830	C	T	20	GENIC	homozygous	112006429
3	112089308	112089309	T	C	30	GENIC	homozygous	112006431
3	112089575	112089576	G	A	20	GENIC	homozygous	111675341
3	112095504	112095505	G	A	24	GENIC	homozygous	111675349
3	112095565	112095566	C	T	29	GENIC	homozygous	112139314
3	112095583	112095584	G	A	28	GENIC	homozygous	112006433
3	112095779	112095780	T	A	24	GENIC	homozygous	112006435
3	112095818	112095819	C	T	18	GENIC	homozygous	112006437
3	112095832	112095833	G	A	17	GENIC	homozygous	112006439
3	112095833	112095834	C	A	18	GENIC	homozygous	112006441
3	112095873	112095874	C	G	20	GENIC	homozygous	112006443
3	112095882	112095883	C	T	22	GENIC	homozygous	112006445
3	112095982	112095983	C	T	17	GENIC	homozygous	112139315
3	112096015	112096016	C	T	16	GENIC	homozygous	112006449
3	112096088	112096089	C	A	22	GENIC	homozygous	112006451
3	112096312	112096313	C	T	8	GENIC	homozygous	112006453
3	112097171	112097172	A	G	11	GENIC	homozygous	112006459
3	112098204	112098205	G	A	26	GENIC	homozygous	112006461
3	112098399	112098400	A	G	21	GENIC	homozygous	111675351
3	112098453	112098454	G	T	14	GENIC	homozygous	111675352
3	112099074	112099075	C	T	14	GENIC	homozygous	119714306
3	112105816	112105817	C	T	20	GENIC	homozygous	112006469
3	112113690	112113691	T	C	16	GENIC	homozygous	112006475
3	112113728	112113729	G	A	16	GENIC	homozygous	112139317
3	112115866	112115867	A	G	15	GENIC	homozygous	111675363
3	112119716	112119717	C	T	20	GENIC	homozygous	111675364
3	112119919	112119920	A	G	14	GENIC	homozygous	112006479