chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	15621213	15621214	C	T	32	GENIC	homozygous	117680504
9	15621513	15621514	T	C	31	GENIC	homozygous	117680506
9	15621580	15621581	A	G	41	GENIC	homozygous	117673062
9	15621721	15621722	C	G	32	GENIC	homozygous	117680508
9	15621871	15621872	A	C	34	GENIC	homozygous	117673066
9	15621892	15621893	C	A	33	GENIC	homozygous	117673068
9	15621937	15621938	T	C	33	GENIC	homozygous	117680510
9	15622201	15622202	A	G	27	GENIC	homozygous	117673072
9	15622426	15622427	A	G	21	GENIC	homozygous	117673076
9	15622818	15622819	T	C	32	GENIC	homozygous	117673078
9	15623957	15623958	C	T	19	GENIC	homozygous	117792140
9	15624170	15624171	G	A	27	GENIC	homozygous	117680512
9	15624227	15624228	C	T	31	GENIC	homozygous	117680514
9	15624265	15624266	G	A	36	GENIC	homozygous	117680516
9	15624894	15624895	A	G	29	GENIC	homozygous	117680518
9	15624943	15624944	G	A	22	GENIC	homozygous	117680520
9	15624994	15624995	C	T	30	GENIC	homozygous	117268034
9	15625151	15625152	A	G	35	GENIC	homozygous	117680522
9	15625336	15625337	A	G	10	GENIC	homozygous	117680524
9	15625635	15625636	C	T	34	GENIC	homozygous	117680526
9	15625879	15625880	T	C	45	GENIC	homozygous	117680528
9	15626581	15626582	C	T	40	GENIC	homozygous	117673102
9	15626662	15626663	A	C	33	GENIC	homozygous	117268035
9	15626672	15626673	T	A	34	GENIC	homozygous	117268036
9	15626688	15626689	A	G	31	GENIC	homozygous	117673104
9	15626986	15626987	C	G	19	GENIC	homozygous	117680530
9	15627219	15627220	C	T	12	GENIC	homozygous	117680532
9	15627431	15627432	C	T	7	GENIC	homozygous	117680534
9	15627858	15627859	C	T	27	GENIC	homozygous	117680536
9	15627990	15627991	C	T	22	GENIC	homozygous	117268037
9	15628012	15628013	A	G	21	GENIC	homozygous	117268038
9	15628427	15628428	C	T	42	GENIC	homozygous	117680538
9	15628492	15628493	T	C	33	GENIC	homozygous	117680540
9	15628951	15628952	A	G	22	GENIC	homozygous	117268040