chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	4699171	4699172	T	TAGACAA	15	GENIC	homozygous	50004803
12	4699181	4699182	C	CA	18	GENIC	heterozygous	50004805
12	4699187	4699188	G	C	14	GENIC	possibly homozygous	50004807
12	4699187	4699188	G	A	7	GENIC	possibly homozygous	50004809
12	4699190	4699191	A	AC	20	GENIC	heterozygous	50004811
12	4699437	4699438	C	A	37	GENIC	homozygous	50004813
12	4699441	4699442	A	G	38	GENIC	homozygous	50004815
12	4699552	4699553	G	A	37	GENIC	homozygous	50004817
12	4699883	4699884	G	A	35	GENIC	homozygous	50004819
12	4700933	4700934	G	A	43	GENIC	homozygous	50004821
12	4701193	4701194	A	T	25	GENIC	homozygous	50004823
12	4701219	4701220	G	A	21	GENIC	homozygous	50004825
12	4701298	4701299	C	T	23	GENIC	homozygous	50004827
12	4701409	4701410	G	A	36	GENIC	homozygous	50004829
12	4702416	4702417	C	T	39	GENIC	homozygous	50004831
12	4702676	4702677	G	A	39	GENIC	homozygous	50004833
12	4704058	4704059	T	TAA	6	GENIC	homozygous	50004835
12	4704684	4704685	T	TC	28	GENIC	homozygous	50004837
12	4705673	4705674	C	A	18	GENIC	homozygous	50004839
12	4705760	4705761	T	C	23	GENIC	homozygous	50004841
12	4705980	4705986	ACACAC	------	1	GENIC	homozygous	50004843
12	4706191	4706192	G	GA	23	GENIC	possibly homozygous	50004847
12	4706949	4706950	A	G	18	GENIC	homozygous	50004849
12	4707380	4707381	G	T	36	GENIC	homozygous	50004851
12	4707559	4707560	A	G	22	GENIC	homozygous	50004853