chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	224380460	224380461	A	AG	13	GENIC	homozygous	57110298
4	224381123	224381124	G	A	10	GENIC	homozygous	57647936
4	224382365	224382366	T	G	21	GENIC	homozygous	57647938
4	224383953	224383956	TCT	---	19	GENIC	homozygous	57110311
4	224384735	224384736	G	A	9	GENIC	homozygous	57647940
4	224384883	224384884	A	C	11	GENIC	homozygous	57647942
4	224385115	224385116	G	A	12	GENIC	homozygous	57647944
4	224385861	224385862	A	G	10	GENIC	homozygous	57647946
4	224387170	224387171	A	G	7	GENIC	homozygous	57647954
4	224387416	224387417	A	C	11	GENIC	homozygous	57647956
4	224387618	224387619	G	T	13	GENIC	homozygous	57647958
4	224387709	224387710	G	A	12	GENIC	homozygous	57647960
4	224387713	224387714	G	C	11	GENIC	homozygous	57647962
4	224388250	224388251	T	TTGA	12	GENIC	homozygous	57110323
4	224388285	224388286	G	-	10	GENIC	homozygous	57647964
4	224389010	224389011	T	A	15	GENIC	homozygous	57647966
4	224389417	224389418	G	T	13	GENIC	homozygous	57647968
4	224390317	224390318	A	-	8	GENIC	homozygous	57647970
4	224390596	224390597	A	G	13	GENIC	homozygous	57110338
4	224391828	224391829	G	T	7	GENIC	homozygous	57647980