chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	14556418	14556419	T	C	31	GENIC	homozygous	111453376
3	14556778	14556779	T	C	22	GENIC	homozygous	111453378
3	14557025	14557026	G	A	26	GENIC	homozygous	111453379
3	14557352	14557353	A	G	17	GENIC	homozygous	111453380
3	14557417	14557418	C	G	20	GENIC	homozygous	111453381
3	14558084	14558085	A	T	12	GENIC	homozygous	111453382
3	14558248	14558249	G	A	16	GENIC	homozygous	111453383
3	14558570	14558571	G	C	36	GENIC	homozygous	119647766
3	14558571	14558572	C	T	37	GENIC	homozygous	111879966
3	14559164	14559165	A	G	21	GENIC	homozygous	111453384
3	14559441	14559442	C	G	26	GENIC	homozygous	111453388
3	14559533	14559534	C	T	24	GENIC	homozygous	119774609
3	14560373	14560374	A	G	23	GENIC	homozygous	111879976
3	14560375	14560376	G	A	22	GENIC	homozygous	111453389
3	14560489	14560490	A	C	18	GENIC	homozygous	111453390
3	14560515	14560516	C	T	17	GENIC	homozygous	112407485
3	14561010	14561011	G	T	27	GENIC	homozygous	111453391
3	14561559	14561560	G	A	35	GENIC	homozygous	119774611
3	14561804	14561805	G	C	31	GENIC	homozygous	111453394
3	14562260	14562261	G	C	15	GENIC	homozygous	111453396
3	14562769	14562770	T	C	30	GENIC	homozygous	111453397
3	14562828	14562829	T	C	28	GENIC	homozygous	111453398
3	14566284	14566285	C	T	13	GENIC	homozygous	111453405
3	14566296	14566297	T	A	11	GENIC	homozygous	119774613
3	14566407	14566408	C	T	17	GENIC	homozygous	111879980
3	14566686	14566687	T	C	26	GENIC	homozygous	119774615
3	14570858	14570859	A	G	20	GENIC	homozygous	111453430
3	14571024	14571025	C	T	29	GENIC	homozygous	119774618
3	14571538	14571539	A	G	20	GENIC	homozygous	111880002
3	14571737	14571738	T	C	22	GENIC	homozygous	119774620