chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
15	103578245	103578246	T	C	49	GENIC	homozygous	112630352
15	103580229	103580230	C	T	22	GENIC	homozygous	112630354
15	103581543	103581544	G	T	37	GENIC	homozygous	112630356
15	103581721	103581722	T	C	27	GENIC	homozygous	112630358
15	103581945	103581946	T	C	47	GENIC	homozygous	112630360
15	103582491	103582492	T	G	38	GENIC	homozygous	112630362
15	103582583	103582584	A	G	36	GENIC	homozygous	112630364
15	103583347	103583348	C	T	35	GENIC	homozygous	112630366
15	103583379	103583380	T	C	29	GENIC	homozygous	112630368
15	103583590	103583591	A	G	36	GENIC	homozygous	112630371
15	103584331	103584332	A	G	21	GENIC	homozygous	118933574
15	103584470	103584471	T	G	3	GENIC	homozygous	119039114
15	103584510	103584511	C	G	14	GENIC	homozygous	118933575
15	103584931	103584932	T	A	21	GENIC	homozygous	112630373
15	103585123	103585124	A	G	24	GENIC	homozygous	118933576
15	103585919	103585920	G	C	26	GENIC	homozygous	112630375
15	103586107	103586108	C	A	28	GENIC	homozygous	112630377
15	103587372	103587373	A	G	46	GENIC	homozygous	112630379
15	103581883	103581884	G	A	32	GENIC	homozygous	113067503
15	103582088	103582089	G	A	31	GENIC	heterozygous	113013203
15	103582121	103582122	T	C	29	GENIC	heterozygous	113280060
15	103582127	103582128	T	C	30	GENIC	heterozygous	113280062
15	103583001	103583002	C	T	34	GENIC	possibly homozygous	119050359
15	103584057	103584058	G	A	26	GENIC	homozygous	119050360
15	103583039	103583040	T	C	31	GENIC	homozygous	112827164
15	103581255	103581256	C	T	21	GENIC	homozygous	112764520