chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	12676898	12676899	T	A	16	GENIC	homozygous	50056857
12	12676917	12676924	GTTTTTG	-------	14	GENIC	possibly homozygous	50056859
12	12676917	12676918	G	-	14	GENIC	heterozygous	50056861
12	12676935	12676936	G	-	9	GENIC	possibly homozygous	50056865
12	12677119	12677120	T	G	25	GENIC	homozygous	50056867
12	12678021	12678022	G	GT	29	GENIC	homozygous	50056871
12	12678450	12678451	T	A	33	GENIC	homozygous	50056873
12	12678452	12678453	T	-	33	GENIC	homozygous	50056875
12	12679240	12679241	G	T	26	GENIC	homozygous	50056877
12	12679743	12679744	G	T	25	GENIC	homozygous	50056879
12	12680142	12680143	A	G	15	GENIC	homozygous	50056881
12	12680459	12680462	GTT	---	17	GENIC	homozygous	50056883
12	12680469	12680470	T	-	19	GENIC	homozygous	50056885
12	12680496	12680514	TATGTGTGTGTGTGTGTG	------------------	10	GENIC	homozygous	50056887
12	12681745	12681750	TTTTT	-----	15	GENIC	heterozygous	50056889
12	12681746	12681750	TTTT	----	15	GENIC	possibly homozygous	50056891
12	12682233	12682234	A	-	23	GENIC	homozygous	50056895
12	12682521	12682522	T	C	18	GENIC	homozygous	50056897
12	12682659	12682660	T	C	18	GENIC	homozygous	50056899
12	12682993	12682994	A	AT	11	GENIC	homozygous	50056901
12	12684313	12684314	C	CT	17	GENIC	homozygous	50056903
12	12684503	12684504	T	C	22	GENIC	homozygous	50056905
12	12684749	12684750	C	T	21	GENIC	homozygous	50056907
12	12684930	12684938	TTTTTTTT	--------	4	GENIC	heterozygous	50363131
12	12684960	12684961	A	G	16	GENIC	homozygous	50056909
12	12676932	12676933	G	C	10	GENIC	possibly homozygous	50531248
12	12676938	12676939	G	T	8	GENIC	possibly homozygous	50531250
12	12677278	12677279	C	CCT	16	GENIC	homozygous	50503803
12	12678454	12678455	T	G	33	GENIC	homozygous	50503804
12	12679980	12679983	AAA	---	7	GENIC	homozygous	50400373
12	12682123	12682125	GT	--	2	GENIC	heterozygous	50556849