chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	248120920	248120921	C		16	GENIC	homozygous	127501686
1	248120949	248120951	AT		20	GENIC	homozygous	127501687
1	248120962	248120962		A	22	GENIC	homozygous	127501688
1	248120966	248120967	C		23	GENIC	homozygous	127501689
1	248120970	248120971	C		24	GENIC	homozygous	127501690
1	248121011	248121012	T		30	GENIC	homozygous	127501691
1	248121016	248121017	A		32	GENIC	homozygous	127501692
1	248121017	248121018	T	C	32	GENIC	homozygous	120515955
1	248121069	248121070	T		21	GENIC	homozygous	130218063
1	248121119	248121120	C	A	22	GENIC	homozygous	108603744
1	248141733	248141733		A	28	GENIC	homozygous	127501709
1	248141738	248141738		G	29	GENIC	homozygous	127501710
1	248141746	248141747	C	A	28	GENIC	homozygous	108603814
1	248141765	248141766	T		26	GENIC	homozygous	127501711
1	248141767	248141768	T		26	GENIC	homozygous	127501712
1	248141795	248141795		GG	26	GENIC	homozygous	127501713
1	248141801	248141801		G	28	GENIC	homozygous	127501714
1	248141813	248141813		GG	29	GENIC	homozygous	127501715
1	248141819	248141819		G	29	GENIC	homozygous	127501716
1	248141825	248141828	TGT		28	GENIC	homozygous	127501717
1	248141829	248141830	T	G	28	GENIC	homozygous	120846646
1	248141834	248141835	T	G	29	GENIC	homozygous	120846647
1	248141836	248141841	TGTTT		28	GENIC	homozygous	127501718
1	248141843	248141843		T	28	GENIC	homozygous	127501719