chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	230790000	230790001	A	G	24	GENIC	homozygous	59432905
2	230790077	230790078	G	A	19	GENIC	homozygous	59432906
2	230790377	230790378	C	T	16	GENIC	homozygous	59432907
2	230790527	230790528	A	G	27	GENIC	homozygous	59432908
2	230790540	230790541	A	AT	26	GENIC	homozygous	59432909
2	230791253	230791254	T	TAA	17	GENIC	homozygous	59432910
2	230791872	230791873	A	G	17	GENIC	homozygous	59432911
2	230792045	230792046	C	CT	13	GENIC	heterozygous	59432912
2	230792971	230792972	A	AT	15	GENIC	possibly homozygous	59432914
2	230792971	230792972	A	ATT	15	GENIC	heterozygous	59432915
2	230794101	230794102	G	GA	28	GENIC	possibly homozygous	59432916
2	230794220	230794221	A	G	14	GENIC	homozygous	59432917
2	230794513	230794523	GTGTGTGTGT	----------	5	GENIC	heterozygous	60594591
2	230794515	230794523	GTGTGTGT	--------	5	GENIC	heterozygous	60520768
2	230794590	230794591	G	-	13	GENIC	homozygous	59432919
2	230795230	230795231	A	AAAAAAG	9	GENIC	homozygous	59432922
2	230795546	230795547	T	C	16	GENIC	homozygous	59432923
2	230795657	230795658	T	C	26	GENIC	homozygous	59432924
2	230796598	230796599	G	A	20	GENIC	homozygous	59432925
2	230796732	230796733	A	G	18	GENIC	homozygous	59432926
2	230799442	230799443	A	G	17	GENIC	homozygous	59432932
2	230800973	230800989	TTTCTTTCTTTCTTTC	----------------	20	GENIC	homozygous	59432933
2	230801068	230801074	TTCCCC	------	19	GENIC	possibly homozygous	59432934
2	230801382	230801383	C	T	20	GENIC	homozygous	59432936