chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	104010084	104010085	A	G	19	GENIC	homozygous	143250155
5	104010205	104010206	T	C	15	GENIC	homozygous	137571381
5	104010250	104010251	G	A	13	GENIC	homozygous	143250156
5	104010991	104010992	A	G	17	GENIC	homozygous	137571382
5	104011391	104011392	G	T	15	GENIC	possibly homozygous	143250157
5	104011900	104011901	T	A	11	GENIC	homozygous	143250158
5	104012815	104012815		T	24	GENIC	possibly homozygous	143184974
5	104013510	104013511	C	T	20	GENIC	homozygous	143250159
5	104013797	104013798	A	G	16	GENIC	homozygous	137571384
5	104015070	104015070		A	21	GENIC	possibly homozygous	143184975
5	104015099	104015100	G		20	GENIC	homozygous	143184976
5	104015103	104015104	C		20	GENIC	homozygous	143184977
5	104015434	104015435	A	G	14	GENIC	homozygous	143250160
5	104015690	104015691	C	T	14	GENIC	homozygous	143250161
5	104016448	104016448		C	16	GENIC	homozygous	143184978
5	104016921	104016922	A	G	22	GENIC	homozygous	143250162
5	104017066	104017066		TGTG	14	GENIC	homozygous	137330116
5	104019029	104019030	T	C	13	GENIC	homozygous	137571389