chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	44897975	44897976	C	T	32	GENIC	homozygous	119674033
3	44898108	44898109	G	A	40	GENIC	homozygous	119648958
3	44899059	44899060	C	T	25	GENIC	homozygous	112441446
3	44899305	44899306	C	T	15	GENIC	homozygous	111553292
3	44899310	44899311	A	G	17	GENIC	homozygous	112441447
3	44899359	44899360	A	G	26	GENIC	homozygous	112441448
3	44901111	44901112	C	G	16	GENIC	homozygous	111553300
3	44901140	44901141	A	G	12	GENIC	homozygous	112441449
3	44901569	44901570	C	T	38	GENIC	homozygous	119674035
3	44902291	44902292	C	A	25	GENIC	homozygous	111553303
3	44902443	44902444	G	A	18	GENIC	homozygous	112441453
3	44903326	44903327	A	T	19	GENIC	homozygous	119674036
3	44903435	44903436	T	C	23	GENIC	homozygous	119674037
3	44903602	44903603	T	C	20	GENIC	homozygous	111553305
3	44905345	44905346	G	A	9	GENIC	homozygous	112419576
3	44905674	44905675	C	T	13	GENIC	homozygous	112419577
3	44905737	44905738	C	A	23	GENIC	homozygous	119674038
3	44905792	44905793	G	C	24	GENIC	homozygous	111553316
3	44906134	44906135	T	A	23	GENIC	homozygous	111553318
3	44906154	44906155	G	C	23	GENIC	homozygous	111553319
3	44907862	44907863	T	C	25	GENIC	homozygous	111553320
3	44909060	44909061	T	C	32	GENIC	homozygous	111553324
3	44909118	44909119	C	T	25	GENIC	homozygous	119674039
3	44909176	44909177	C	T	18	GENIC	homozygous	112419589
3	44909899	44909900	A	G	24	GENIC	homozygous	111553326
3	44909927	44909928	A	C	24	GENIC	homozygous	111553327
3	44910562	44910563	A	G	23	GENIC	homozygous	111553331
3	44910890	44910891	C	G	20	GENIC	homozygous	119674040
3	44911548	44911549	A	G	25	GENIC	homozygous	111553336
3	44915526	44915527	A	T	23	GENIC	homozygous	111553353
3	44916907	44916908	C	T	25	GENIC	homozygous	119674041
3	44917894	44917895	C	A	24	GENIC	homozygous	111553369
3	44919448	44919449	A	G	26	GENIC	homozygous	111553376
3	44927537	44927538	G	T	17	GENIC	homozygous	112419593
3	44931361	44931362	A	G	32	GENIC	homozygous	111553384