chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30180066	30180066		T	38	GENIC	homozygous	127607275
2	30180073	30180074	C		35	GENIC	homozygous	127607276
2	30180076	30180077	G	A	34	GENIC	homozygous	120122962
2	30180084	30180084		C	37	GENIC	homozygous	127607277
2	30180081	30180082	C	T	37	GENIC	homozygous	109672753
2	30180100	30180101	C	T	40	GENIC	homozygous	109672755
2	30182001	30182001		G	51	GENIC	homozygous	127607278
2	30183293	30183294	T		30	GENIC	homozygous	127607279
2	30188370	30188371	A	G	10	GENIC	homozygous	109672775
2	30188399	30188400	C	T	11	GENIC	homozygous	109672777
2	30198550	30198551	G	A	39	GENIC	heterozygous	127785860
2	30198555	30198556	A	G	39	GENIC	heterozygous	127785861
2	30201551	30201552	C	T	32	GENIC	homozygous	109672829
2	30201658	30201662	CCCC		41	GENIC	homozygous	127607283
2	30201663	30201663		AAT	42	GENIC	homozygous	127607284
2	30207831	30207832	T		6	GENIC	homozygous	129863666
2	30207847	30207848	C		11	GENIC	homozygous	129863667
2	30207855	30207855		C	13	GENIC	homozygous	129863668
2	30207857	30207864	CCATAGA		13	GENIC	homozygous	129863669
2	30195449	30195452	CCT		19	GENIC	heterozygous	135148299
2	30198515	30198516	G	A	37	GENIC	heterozygous	132388183
2	30201576	30201577	A		29	GENIC	heterozygous	130630643
2	30207843	30207844	A	C	11	GENIC	homozygous	120165314
2	30213630	30213631	G	A	43	GENIC	heterozygous	110500779
2	30213631	30213632	G	T	41	GENIC	heterozygous	110500781
2	30213633	30213634	T	A	41	GENIC	heterozygous	110500783
2	30213656	30213657	A	G	43	GENIC	heterozygous	109672865
2	30213661	30213662	C	T	42	GENIC	heterozygous	109672867
2	30213669	30213670	G	A	42	GENIC	heterozygous	109672869
2	30233786	30233854	ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA		19	GENIC	homozygous	130244041
2	30234516	30234516		GTG	26	GENIC	possibly homozygous	130860654