chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	157503289	157503290	G	C	22	GENIC	homozygous	119186240
5	157503293	157503294	C	T	23	GENIC	homozygous	119186241
5	157503519	157503520	T	C	20	GENIC	homozygous	119186242
5	157503621	157503622	C	T	21	GENIC	homozygous	119186243
5	157503850	157503851	A	C	24	GENIC	homozygous	119186244
5	157503887	157503888	C	T	27	GENIC	homozygous	119186245
5	157503909	157503910	A	G	21	GENIC	homozygous	119186246
5	157504766	157504767	C	T	22	GENIC	possibly homozygous	119186247
5	157505353	157505354	A	C	28	GENIC	possibly homozygous	119186248
5	157505358	157505359	A	G	27	GENIC	possibly homozygous	119186249
5	157505418	157505419	T	C	32	GENIC	possibly homozygous	119186250
5	157505504	157505505	A	G	26	GENIC	homozygous	119186251
5	157505507	157505508	A	G	24	GENIC	homozygous	114069939
5	157505563	157505564	G	A	29	GENIC	possibly homozygous	119186252
5	157507439	157507440	A	G	23	GENIC	possibly homozygous	114069944
5	157508120	157508121	G	A	34	GENIC	possibly homozygous	119186253
5	157508442	157508443	A	G	33	GENIC	possibly homozygous	119186254
5	157509705	157509706	C	T	12	GENIC	homozygous	114069947
5	157509809	157509810	A	G	28	GENIC	homozygous	114069948
5	157510465	157510466	C	T	23	GENIC	homozygous	119186255
5	157511163	157511164	T	C	29	GENIC	homozygous	119186256
5	157511418	157511419	T	G	21	GENIC	homozygous	119204616
5	157512498	157512499	A	G	32	GENIC	homozygous	119186257
5	157516221	157516222	T	C	26	GENIC	possibly homozygous	119186258
5	157516293	157516294	T	C	23	GENIC	possibly homozygous	119186259
5	157516301	157516302	A	G	25	GENIC	possibly homozygous	119186260
5	157516335	157516336	C	A	28	GENIC	possibly homozygous	119186261