chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	227273097	227273098	A	G	18	GENIC	homozygous	130275908
2	227275787	227275788	T	G	5	GENIC	heterozygous	130275909
2	227275859	227275860	A	G	5	GENIC	heterozygous	130275910
2	227275905	227275906	C	T	5	GENIC	heterozygous	130275911
2	227276198	227276199	A	T	20	GENIC	heterozygous	111288331
2	227278791	227278792	T	A	14	GENIC	heterozygous	130275912
2	227303598	227303598		C	49	GENIC	homozygous	127744013
2	227303600	227303600		G	50	GENIC	homozygous	127744014
2	227373466	227373466		A	37	GENIC	homozygous	127744048
2	227373467	227373467		C	37	GENIC	homozygous	127744049
2	227373472	227373473	T	A	38	GENIC	homozygous	110280872
2	227373477	227373478	A	T	39	GENIC	homozygous	110280874
2	227373482	227373483	A		37	GENIC	homozygous	127744050
2	227373485	227373486	G		36	GENIC	homozygous	127744051
2	227373538	227373538		T	24	GENIC	homozygous	127744052
2	227373562	227373563	T		22	GENIC	homozygous	127744053
2	227373581	227373584	ATA		22	GENIC	homozygous	127744054
2	227373686	227373686		C	2	GENIC	homozygous	127744057
2	227373709	227373709		A	2	GENIC	homozygous	127744058
2	227390416	227390417	T	C	17	GENIC	homozygous	120161359
2	227390419	227390420	T	C	17	GENIC	homozygous	120131100
2	227390428	227390429	A	C	17	GENIC	homozygous	110281021
2	227390463	227390464	T		13	GENIC	homozygous	127744068
2	227392598	227392599	G	T	40	GENIC	homozygous	120131103
2	227392600	227392602	GG		39	GENIC	homozygous	127744071
2	227392607	227392613	GTGAAA		40	GENIC	homozygous	127744072
2	227373521	227373522	C		29	GENIC	homozygous	130532759
2	227373620	227373623	CAT		8	GENIC	heterozygous	130255150