chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30180066	30180066		T	51	GENIC	homozygous	127607275
2	30180073	30180074	C		52	GENIC	homozygous	127607276
2	30180076	30180077	G	A	50	GENIC	homozygous	120122962
2	30180081	30180082	C	T	51	GENIC	homozygous	109672753
2	30180084	30180084		C	48	GENIC	homozygous	127607277
2	30180100	30180101	C	T	43	GENIC	homozygous	109672755
2	30182001	30182001		G	36	GENIC	homozygous	127607278
2	30183293	30183294	T		24	GENIC	homozygous	127607279
2	30188370	30188371	A	G	8	GENIC	heterozygous	109672775
2	30188399	30188400	C	T	11	GENIC	heterozygous	109672777
2	30188736	30188737	T	G	26	GENIC	heterozygous	109672787
2	30188740	30188741	C	T	25	GENIC	heterozygous	109672789
2	30188751	30188753	AT		26	GENIC	heterozygous	130739487
2	30188757	30188760	ATA		29	GENIC	heterozygous	130739488
2	30188777	30188778	A	G	29	GENIC	heterozygous	110928677
2	30198550	30198551	G	A	37	GENIC	heterozygous	127785860
2	30198555	30198556	A	G	35	GENIC	heterozygous	127785861
2	30201551	30201552	C	T	36	GENIC	homozygous	109672829
2	30201576	30201577	A		32	GENIC	heterozygous	130630643
2	30201658	30201662	CCCC		44	GENIC	homozygous	127607283
2	30201663	30201663		AAT	44	GENIC	homozygous	127607284
2	30207831	30207832	T		7	GENIC	homozygous	129863666
2	30207847	30207848	C		9	GENIC	homozygous	129863667
2	30207855	30207855		C	13	GENIC	homozygous	129863668
2	30207857	30207864	CCATAGA		15	GENIC	homozygous	129863669
2	30213630	30213631	G	A	57	GENIC	heterozygous	110500779
2	30213631	30213632	G	T	58	GENIC	heterozygous	110500781
2	30213633	30213634	T	A	58	GENIC	heterozygous	110500783
2	30234516	30234516		GTG	17	GENIC	possibly homozygous	130860654
2	30233786	30233854	ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA		15	GENIC	homozygous	130244041
2	30207843	30207844	A	C	9	GENIC	homozygous	120165314
2	30214096	30214097	T	C	38	GENIC	homozygous	134801777