chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	14215920	14215921	G	A	27	GENIC	homozygous	116736848
10	14215943	14215944	T	C	25	GENIC	homozygous	116736849
10	14217589	14217589		T	16	GENIC	possibly homozygous	131087988
10	14218046	14218047	T	C	13	GENIC	homozygous	116736850
10	14218193	14218193		AT	10	GENIC	homozygous	131087989
10	14218323	14218324	A		8	GENIC	homozygous	131087990
10	14218612	14218613	G	A	21	GENIC	homozygous	116994684
10	14218854	14218855	C	A	13	GENIC	homozygous	116736851
10	14221318	14221319	G	C	17	GENIC	homozygous	116736852
10	14223190	14223191	T	C	16	GENIC	homozygous	116736853
10	14225100	14225100		TGTGTGTGTAGTATGTGG	10	GENIC	homozygous	131087991
10	14227738	14227739	A	G	18	GENIC	homozygous	116736854
10	14228221	14228222	T	C	14	GENIC	homozygous	116736855
10	14228922	14228926	TTTG		21	GENIC	homozygous	131087992
10	14229314	14229315	G	A	16	GENIC	homozygous	116736856