chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	59490878	59490879	T	A	17	GENIC	homozygous	119163684
5	59492425	59492426	A	G	15	GENIC	homozygous	113821655
5	59496242	59496243	A	G	31	GENIC	homozygous	113821665
5	59496492	59496493	C	A	14	GENIC	homozygous	119163686
5	59496507	59496508	G	A	12	GENIC	homozygous	119163688
5	59498256	59498257	G	A	32	GENIC	homozygous	119163690
5	59499643	59499644	T	A	29	GENIC	homozygous	119163692
5	59500179	59500180	A	G	21	GENIC	homozygous	113821673
5	59501607	59501608	C	T	23	GENIC	homozygous	119163694
5	59502207	59502208	C	A	27	GENIC	homozygous	113821681
5	59502243	59502244	C	T	23	GENIC	homozygous	113821683
5	59502300	59502301	G	A	29	GENIC	homozygous	113821685
5	59502683	59502684	T	C	21	GENIC	homozygous	113821691
5	59502698	59502699	A	T	21	GENIC	homozygous	113821693
5	59503232	59503233	C	T	20	GENIC	homozygous	113821701
5	59503245	59503246	C	T	21	GENIC	homozygous	113821703
5	59503422	59503423	G	A	21	GENIC	homozygous	114206846
5	59503514	59503515	T	C	19	GENIC	homozygous	113821707
5	59504116	59504117	T	C	12	GENIC	homozygous	113821711
5	59504488	59504489	A	G	18	GENIC	homozygous	113821713
5	59504831	59504832	C	A	24	GENIC	homozygous	119163696
5	59504888	59504889	T	C	28	GENIC	homozygous	113821715
5	59505019	59505020	G	T	26	GENIC	homozygous	119163698
5	59505062	59505063	T	A	22	GENIC	homozygous	119163700
5	59505193	59505194	T	C	23	GENIC	homozygous	119163702
5	59505463	59505464	T	C	13	GENIC	homozygous	113821719
5	59505702	59505703	C	T	22	GENIC	homozygous	119163704
5	59505718	59505719	G	A	16	GENIC	homozygous	113821721
5	59505848	59505849	C	T	18	GENIC	homozygous	119163706
5	59505925	59505926	T	C	17	GENIC	homozygous	119163708
5	59506002	59506003	C	T	23	GENIC	homozygous	119163710
5	59506256	59506257	C	T	16	GENIC	homozygous	119163712
5	59506991	59506992	G	C	16	GENIC	homozygous	119163714