chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	6256467	6256468	T	C	12	GENIC	homozygous	50017693
12	6256470	6256471	G	GA	11	GENIC	heterozygous	50017695
12	6256473	6256474	A	AC	11	GENIC	possibly homozygous	50017697
12	6256493	6256494	T	TCC	16	GENIC	heterozygous	50503337
12	6256495	6256497	AA	--	16	GENIC	heterozygous	50503338
12	6256630	6256631	C	-	1	GENIC	homozygous	50503339
12	6256646	6256647	T	C	2	GENIC	homozygous	50017711
12	6256914	6256915	A	T	15	GENIC	homozygous	50017713
12	6257035	6257036	C	T	20	GENIC	possibly homozygous	50017715
12	6257188	6257189	A	G	17	GENIC	possibly homozygous	50017717
12	6257275	6257276	C	A	10	GENIC	heterozygous	50017719
12	6257302	6257303	A	G	1	GENIC	homozygous	50017721
12	6257308	6257309	T	A	2	GENIC	heterozygous	50017723
12	6257322	6257323	T	A	8	GENIC	homozygous	50017725
12	6257410	6257411	T	C	16	GENIC	homozygous	50017727
12	6257685	6257686	G	C	14	GENIC	possibly homozygous	50017729
12	6257742	6257743	C	G	17	GENIC	homozygous	50017731
12	6258068	6258069	G	A	5	GENIC	homozygous	50017733
12	6258537	6258538	C	T	12	GENIC	possibly homozygous	50017747
12	6259105	6259106	A	G	5	GENIC	homozygous	50017757
12	6259157	6259158	C	T	16	GENIC	homozygous	50017759
12	6259187	6259188	T	C	14	GENIC	possibly homozygous	50017761
12	6259251	6259252	A	G	9	GENIC	possibly homozygous	50017763
12	6259293	6259297	TGTT	----	5	GENIC	heterozygous	50017765
12	6259378	6259379	T	TA	5	GENIC	heterozygous	50017767
12	6259450	6259451	G	A	9	GENIC	homozygous	50017769
12	6259580	6259581	A	G	11	GENIC	homozygous	50017771
12	6259791	6259792	T	C	12	GENIC	homozygous	50017773
12	6259986	6259987	A	ATT	4	GENIC	heterozygous	50017789
12	6259986	6259987	A	AT	4	GENIC	heterozygous	50503340
12	6260020	6260021	A	G	16	GENIC	homozygous	50017791
12	6260057	6260058	T	G	19	GENIC	possibly homozygous	50017793
12	6260262	6260269	AATAGAG	-------	11	GENIC	heterozygous	50017797
12	6260309	6260310	C	T	15	GENIC	possibly homozygous	50017799
12	6260325	6260326	A	C	10	GENIC	homozygous	50017801
12	6260566	6260567	C	T	27	GENIC	homozygous	50017807
12	6260602	6260603	G	A	23	GENIC	possibly homozygous	50017811
12	6260707	6260708	A	G	14	GENIC	homozygous	50017817
12	6260890	6260891	G	A	18	GENIC	homozygous	50017835
12	6261193	6261194	A	G	18	GENIC	homozygous	50017847
12	6261384	6261391	GGGGTGG	-------	13	GENIC	heterozygous	50503341
12	6261390	6261391	G	GCTT	12	GENIC	heterozygous	50503342
12	6261426	6261427	C	T	16	GENIC	homozygous	50017861
12	6261459	6261460	G	GT	17	GENIC	homozygous	50017865
12	6261629	6261630	A	G	21	GENIC	heterozygous	50017867
12	6261983	6261984	A	AT	12	GENIC	homozygous	50017879
12	6261996	6261997	G	T	8	GENIC	homozygous	50017881
12	6261997	6261998	A	T	8	GENIC	homozygous	50017883
12	6262048	6262049	C	T	13	GENIC	heterozygous	50017885
12	6262069	6262070	T	C	24	GENIC	homozygous	50017887
12	6262623	6262624	G	A	21	GENIC	homozygous	50017891
12	6262800	6262801	C	T	15	GENIC	possibly homozygous	50017893
12	6262838	6262839	T	G	12	GENIC	homozygous	50017895
12	6262844	6262845	C	A	14	GENIC	possibly homozygous	50017897
12	6262889	6262890	A	G	22	GENIC	possibly homozygous	50017899
12	6263298	6263299	G	A	21	GENIC	homozygous	50017913
12	6263371	6263372	C	T	19	GENIC	possibly homozygous	50017915