chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	47519020	47519021	T	C	19	GENIC	homozygous	59681299
2	47519268	47519269	A	C	2	GENIC	homozygous	59681303
2	47519295	47519296	T	C	10	GENIC	possibly homozygous	59681305
2	47519422	47519423	G	-	11	GENIC	possibly homozygous	59681307
2	47519573	47519574	C	T	14	GENIC	homozygous	59681309
2	47519714	47519715	T	C	3	GENIC	homozygous	59681311
2	47519880	47519881	T	C	16	GENIC	homozygous	59681313
2	47519917	47519918	C	A	9	GENIC	homozygous	59681315
2	47519936	47519937	A	G	6	GENIC	homozygous	59681317
2	47519945	47519946	A	G	6	GENIC	homozygous	59681319
2	47519994	47519995	A	G	14	GENIC	heterozygous	59681321
2	47520274	47520275	T	A	17	GENIC	homozygous	58799296
2	47520582	47520583	T	C	27	GENIC	possibly homozygous	59681327
2	47520680	47520681	T	A	17	GENIC	possibly homozygous	59681329
2	47520836	47520837	C	T	30	GENIC	possibly homozygous	59681331
2	47521145	47521146	G	A	11	GENIC	homozygous	59681333
2	47521194	47521195	T	TGCGGGGG	3	GENIC	heterozygous	61533103
2	47521198	47521199	A	G	2	GENIC	homozygous	59681335
2	47521203	47521204	T	G	1	GENIC	homozygous	59681337
2	47521338	47521339	C	T	14	GENIC	homozygous	58799301
2	47521718	47521722	AGAG	----	9	GENIC	homozygous	59681341
2	47521970	47521971	A	G	9	GENIC	heterozygous	59681343
2	47522113	47522114	A	G	12	GENIC	homozygous	59681345
2	47522641	47522642	A	-	18	GENIC	possibly homozygous	59681347
2	47523034	47523035	C	T	18	GENIC	possibly homozygous	59681349
2	47523126	47523127	C	CATTT	2	GENIC	homozygous	59681351
2	47523633	47523634	T	TAAG	7	GENIC	homozygous	59681353
2	47523854	47523855	A	-	11	GENIC	homozygous	59681355
2	47523999	47524000	G	A	23	GENIC	possibly homozygous	59681357
2	47524050	47524051	A	AGTT	11	GENIC	homozygous	59681359
2	47524558	47524559	T	G	16	GENIC	possibly homozygous	59681361
2	47524734	47524735	T	C	17	GENIC	homozygous	59681363
2	47524768	47524769	T	C	23	GENIC	heterozygous	59681365