chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31962110	31962111	C	CCA	23	GENIC	homozygous	50442226
12	31962159	31962160	G	A	27	GENIC	homozygous	50442228
12	31962199	31962200	C	-	37	GENIC	homozygous	50442230
12	31962766	31962767	A	G	37	GENIC	homozygous	50442232
12	31963086	31963087	G	A	44	GENIC	homozygous	50442234
12	31963798	31963799	C	CCCGA	29	GENIC	homozygous	50442236
12	31964976	31964977	C	T	37	GENIC	homozygous	50442240
12	31965111	31965112	G	A	27	GENIC	homozygous	50442242
12	31965360	31965361	C	T	16	GENIC	homozygous	50442244
12	31965949	31965950	C	T	39	GENIC	homozygous	50442246
12	31966322	31966323	G	GGTGTGTGT	18	GENIC	heterozygous	50615116
12	31966322	31966323	G	GGTGTGTGTGTGTGT	18	GENIC	possibly homozygous	50609711
12	31966416	31966417	T	-	31	GENIC	homozygous	50442248
12	31966494	31966495	A	G	38	GENIC	possibly homozygous	50442250
12	31966523	31966524	A	C	47	GENIC	possibly homozygous	50591516
12	31966524	31966525	C	A	47	GENIC	possibly homozygous	50591517
12	31966670	31966671	G	A	40	GENIC	homozygous	50442252
12	31966692	31966693	C	T	40	GENIC	homozygous	50442254
12	31966977	31966978	A	G	26	GENIC	homozygous	50442256
12	31967053	31967054	C	A	24	GENIC	homozygous	50442258
12	31967141	31967142	C	T	38	GENIC	homozygous	50442260
12	31967158	31967163	AATAC	-----	35	GENIC	homozygous	50442262
12	31967305	31967306	T	C	27	GENIC	homozygous	50442264
12	31967330	31967331	A	G	37	GENIC	homozygous	50442266
12	31967881	31967882	T	G	33	GENIC	homozygous	50442268
12	31967951	31967952	A	G	24	GENIC	homozygous	50442270
12	31968259	31968260	A	C	49	GENIC	homozygous	50174766
12	31968853	31968854	T	TA	20	GENIC	possibly homozygous	50312734
12	31968993	31969008	TATTATTATTATTAT	---------------	9	GENIC	homozygous	50609712
12	31969283	31969284	T	TTCACGTCGGGAGC	40	GENIC	homozygous	50442272
12	31970085	31970086	G	A	43	GENIC	homozygous	50442274
12	31970549	31970550	C	T	31	GENIC	homozygous	50442276
12	31969608	31969609	C	CA	8	GENIC	heterozygous	50558362