chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4699171	4699172	T	TAGACAA	31	GENIC	homozygous	50004803
12	4699187	4699188	G	C	34	GENIC	possibly homozygous	50004807
12	4699441	4699442	A	G	32	GENIC	homozygous	50004815
12	4699552	4699553	G	A	30	GENIC	homozygous	50004817
12	4699689	4699690	C	T	43	GENIC	homozygous	50394995
12	4699883	4699884	G	A	34	GENIC	homozygous	50004819
12	4700933	4700934	G	A	30	GENIC	homozygous	50004821
12	4701193	4701194	A	T	12	GENIC	homozygous	50004823
12	4701219	4701220	G	A	12	GENIC	homozygous	50004825
12	4701298	4701299	C	T	27	GENIC	homozygous	50004827
12	4701409	4701410	G	A	38	GENIC	homozygous	50004829
12	4702416	4702417	C	T	29	GENIC	homozygous	50004831
12	4702676	4702677	G	A	33	GENIC	homozygous	50004833
12	4704018	4704019	T	C	10	GENIC	homozygous	50394997
12	4704033	4704034	T	C	6	GENIC	homozygous	50394999
12	4704134	4704135	C	T	12	GENIC	homozygous	50395001
12	4704283	4704284	T	C	34	GENIC	homozygous	50395003
12	4705806	4705807	C	T	30	GENIC	possibly homozygous	50395007
12	4705979	4705980	T	TAC	20	GENIC	heterozygous	50555893
12	4705979	4705980	T	TACACAC	20	GENIC	possibly homozygous	50526690
12	4705979	4705980	T	TACACACAC	20	GENIC	heterozygous	50567225
12	4706949	4706950	A	G	23	GENIC	homozygous	50004849
12	4707770	4707771	G	GCC	5	GENIC	homozygous	50526692
12	4707774	4707775	G	GC	5	GENIC	homozygous	50526694
12	4707775	4707776	G	GCGCCC	5	GENIC	homozygous	50526696
12	4708031	4708032	C	T	41	GENIC	homozygous	50395009