chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10261094	10261095	C	T	68	GENIC	possibly homozygous	130051715
20	10261706	10261707	C	G	40	GENIC	possibly homozygous	155134331
20	10261706	10261707	C		40	GENIC	heterozygous	403464015
20	10261804	10261805	A	G	50	GENIC	homozygous	130051716
20	10262231	10262232	C	T	53	GENIC	possibly homozygous	130051717
20	10262356	10262357	T	C	56	GENIC	homozygous	130051718
20	10262477	10262478	C	T	52	GENIC	homozygous	130051719
20	10262554	10262555	C	T	57	GENIC	homozygous	130051720
20	10263709	10263710	C	T	60	GENIC	homozygous	130051721
20	10264637	10264638	T	C	57	GENIC	homozygous	130051722
20	10264704	10264705	A	G	57	GENIC	homozygous	130051723
20	10265757	10265758	T	C	69	GENIC	homozygous	130051724
20	10266589	10266590	C	T	64	GENIC	homozygous	130051725
20	10266811	10266812	A	G	61	GENIC	homozygous	130051726
20	10267544	10267545	T	C	57	GENIC	homozygous	130051727
20	10267578	10267579	T	C	56	GENIC	homozygous	130051728
20	10267595	10267597	CC		55	GENIC	homozygous	129982698
20	10267866	10267867	C	A	60	GENIC	homozygous	130051729
20	10268294	10268295	C	T	65	GENIC	homozygous	130051730
20	10269311	10269312	C	T	59	GENIC	homozygous	130051731
20	10270603	10270604	A	G	59	GENIC	homozygous	130051732
20	10271419	10271420	T	C	69	GENIC	homozygous	130051733
20	10271600	10271601	T	G	77	GENIC	homozygous	130051734
20	10269739	10269739		CCCAGC	48	GENIC	homozygous	129982699