chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	157247631	157247632	G	T	30	GENIC	homozygous	114069291
5	157248770	157248771	A	C	27	GENIC	homozygous	114452250
5	157248814	157248815	G	A	25	GENIC	homozygous	114452252
5	157249288	157249289	A	G	36	GENIC	homozygous	114069292
5	157249468	157249469	C	T	17	GENIC	homozygous	114452254
5	157250146	157250147	C	T	37	GENIC	homozygous	114452256
5	157251501	157251502	C	A	31	GENIC	homozygous	114452258
5	157251617	157251618	A	G	30	GENIC	possibly homozygous	114452260
5	157251778	157251779	A	C	24	GENIC	homozygous	114069296
5	157251953	157251954	T	C	33	GENIC	homozygous	114069297
5	157252251	157252252	T	C	39	GENIC	homozygous	114452262
5	157254282	157254283	A	G	25	GENIC	homozygous	114452266
5	157254331	157254332	A	C	31	GENIC	homozygous	114452268
5	157254586	157254587	T	C	27	GENIC	homozygous	114069305
5	157254587	157254588	G	A	28	GENIC	homozygous	114069306
5	157254596	157254597	C	A	26	GENIC	homozygous	114452270
5	157254618	157254619	T	G	26	GENIC	homozygous	114452272
5	157255531	157255532	G	A	44	GENIC	homozygous	114069309
5	157255825	157255826	A	G	34	GENIC	homozygous	114452274
5	157256788	157256789	A	T	37	GENIC	homozygous	114452276
5	157259659	157259660	A	C	42	GENIC	homozygous	114069314
5	157261761	157261762	A	C	36	GENIC	homozygous	114452278
5	157262378	157262379	A	G	38	GENIC	homozygous	114069316
5	157268052	157268053	T	C	28	GENIC	homozygous	114069326