chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	104185593	104185594	C	T	19	GENIC	homozygous	108904702
1	104186011	104186012	A	G	21	GENIC	homozygous	108904703
1	104186938	104186939	A	G	26	GENIC	heterozygous	108904704
1	104186989	104186990	A	T	27	GENIC	homozygous	108904705
1	104188126	104188127	A	G	19	GENIC	homozygous	108904706
1	104188215	104188216	A	C	27	GENIC	homozygous	108904707
1	104188616	104188617	T	C	22	GENIC	homozygous	108904708
1	104189183	104189184	G	A	25	GENIC	homozygous	108904709
1	104189885	104189886	T	C	27	GENIC	homozygous	108904710
1	104191775	104191776	G	A	15	GENIC	homozygous	108904711
1	104192553	104192554	C	T	22	GENIC	homozygous	108904712
1	104198624	104198625	T	A	54	GENIC	homozygous	108165706
1	104198438	104198439	C	A	16	GENIC	homozygous	108165705
1	104198629	104198630	C	T	57	GENIC	heterozygous	108165707
1	104198694	104198695	A	C	71	GENIC	heterozygous	108165708
1	104198705	104198706	C	A	52	GENIC	homozygous	108165709
1	104200575	104200576	C	A	21	GENIC	homozygous	108904713
1	104200579	104200580	T	A	20	GENIC	homozygous	108904714
1	104201321	104201322	C	G	28	GENIC	homozygous	108165710
1	104201340	104201341	C	A	29	GENIC	homozygous	108165711
1	104201720	104201721	A	C	26	GENIC	homozygous	108904715
1	104201906	104201907	T	C	20	GENIC	homozygous	108904716
1	104203387	104203388	C	A	9	GENIC	possibly homozygous	108904717