chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157613725	157613726	G	A	46	GENIC	homozygous	112906742
4	157613853	157613854	G	T	32	GENIC	homozygous	112906744
4	157614185	157614186	T	G	31	GENIC	homozygous	112906746
4	157616535	157616536	C	A	20	GENIC	homozygous	112906752
4	157619978	157619979	G	T	14	GENIC	homozygous	112906754
4	157620744	157620745	T	C	23	GENIC	homozygous	112906756
4	157621147	157621148	C	T	26	GENIC	homozygous	112906758
4	157623083	157623084	G	A	28	GENIC	homozygous	112906760
4	157626447	157626448	T	C	36	GENIC	homozygous	112906764
4	157627043	157627044	T	C	24	GENIC	homozygous	112906766
4	157629525	157629526	T	C	25	GENIC	homozygous	112906768
4	157631950	157631951	A	G	23	GENIC	homozygous	112906772
4	157632657	157632658	T	C	26	GENIC	homozygous	112906774
4	157633500	157633501	A	G	27	GENIC	homozygous	112906776
4	157634098	157634099	T	C	22	GENIC	homozygous	112906778
4	157635239	157635240	A	C	24	GENIC	homozygous	112906780
4	157635295	157635296	C	T	25	GENIC	homozygous	112906782
4	157638495	157638496	T	C	23	GENIC	homozygous	112906784
4	157639657	157639658	G	C	17	GENIC	homozygous	112906786
4	157644216	157644217	C	G	17	GENIC	homozygous	112906788
4	157644340	157644341	T	C	25	GENIC	homozygous	112906790