chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157613725	157613726	G	A	56	GENIC	possibly homozygous	112906742
4	157613853	157613854	G	T	59	GENIC	homozygous	112906744
4	157614185	157614186	T	G	50	GENIC	homozygous	112906746
4	157614774	157614775	A	T	66	GENIC	homozygous	112906748
4	157614977	157614978	A	C	41	GENIC	homozygous	112906750
4	157616535	157616536	C	A	68	GENIC	homozygous	112906752
4	157619978	157619979	G	T	38	GENIC	homozygous	112906754
4	157620744	157620745	T	C	52	GENIC	homozygous	112906756
4	157621147	157621148	C	T	45	GENIC	homozygous	112906758
4	157623083	157623084	G	A	65	GENIC	homozygous	112906760
4	157625710	157625711	C	T	55	GENIC	homozygous	112906762
4	157626447	157626448	T	C	60	GENIC	homozygous	112906764
4	157627043	157627044	T	C	45	GENIC	homozygous	112906766
4	157628913	157628913		GT	59	GENIC	homozygous	128096211
4	157629525	157629526	T	C	51	GENIC	homozygous	112906768
4	157630918	157630919	G	T	35	GENIC	homozygous	112906770
4	157631950	157631951	A	G	55	GENIC	homozygous	112906772
4	157632657	157632658	T	C	59	GENIC	homozygous	112906774
4	157633500	157633501	A	G	59	GENIC	homozygous	112906776
4	157633855	157633859	TGTC		57	GENIC	homozygous	128096212
4	157634098	157634099	T	C	48	GENIC	homozygous	112906778
4	157635239	157635240	A	C	68	GENIC	possibly homozygous	112906780
4	157635295	157635296	C	T	55	GENIC	possibly homozygous	112906782
4	157637454	157637460	CCCCTG		36	GENIC	homozygous	128096213
4	157637690	157637708	CAGGAGGGAGGGTGCAGC		47	GENIC	homozygous	128096214
4	157638495	157638496	T	C	55	GENIC	homozygous	112906784
4	157639366	157639366		C	49	GENIC	homozygous	128096215
4	157639657	157639658	G	C	47	GENIC	homozygous	112906786
4	157644216	157644217	C	G	68	GENIC	homozygous	112906788
4	157644340	157644341	T	C	48	GENIC	homozygous	112906790