chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	30180066	30180066		T	39	GENIC	homozygous	127607275
2	30180073	30180074	C		42	GENIC	homozygous	127607276
2	30180076	30180077	G	A	43	GENIC	homozygous	120122962
2	30180081	30180082	C	T	40	GENIC	homozygous	109672753
2	30180084	30180084		C	41	GENIC	homozygous	127607277
2	30180100	30180101	C	T	44	GENIC	homozygous	109672755
2	30182001	30182001		G	46	GENIC	homozygous	127607278
2	30183293	30183294	T		26	GENIC	homozygous	127607279
2	30188370	30188371	A	G	9	GENIC	homozygous	109672775
2	30188399	30188400	C	T	12	GENIC	homozygous	109672777
2	30201551	30201552	C	T	39	GENIC	homozygous	109672829
2	30201658	30201662	CCCC		52	GENIC	homozygous	127607283
2	30201663	30201663		AAT	52	GENIC	homozygous	127607284
2	30207831	30207832	T		5	GENIC	homozygous	129863666
2	30207847	30207848	C		5	GENIC	homozygous	129863667
2	30207855	30207855		C	5	GENIC	homozygous	129863668
2	30207857	30207864	CCATAGA		5	GENIC	homozygous	129863669
2	30189780	30189781	T	C	52	GENIC	homozygous	111098066
2	30207843	30207844	A	C	5	GENIC	homozygous	120165314
2	30234516	30234516		GTG	12	GENIC	homozygous	130860654
2	30236636	30236637	C	T	48	GENIC	homozygous	120165315
2	30241574	30241574		G	31	GENIC	homozygous	127607339
2	30241576	30241577	A		33	GENIC	homozygous	127607340
2	30241592	30241593	C		43	GENIC	homozygous	127607341
2	30241607	30241607		T	48	GENIC	homozygous	127607342
2	30241621	30241622	G		51	GENIC	homozygous	127607343
2	30241654	30241655	C		49	GENIC	homozygous	127607344
2	30241667	30241668	C	T	46	GENIC	homozygous	109673333
2	30241672	30241673	A		46	GENIC	homozygous	127607345
2	30241680	30241682	TA		47	GENIC	homozygous	127607346
2	30241692	30241692		C	48	GENIC	homozygous	127607347
2	30241719	30241719		GTCTAACTCCATTTC	53	GENIC	homozygous	127607348
2	30233786	30233854	ATGTAGCCTGGCTGTCTTGCCCAACCAGAACCTCACGCGGTTCTTGAAACTTTGGATACAGACCCTTA		16	GENIC	homozygous	130244041