chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157359381	157359382	T	C	50	GENIC	homozygous	112905999
4	157359635	157359636	A	T	41	GENIC	homozygous	112906001
4	157359881	157359882	G	T	49	GENIC	homozygous	112906003
4	157359944	157359945	G	A	45	GENIC	homozygous	112906005
4	157360418	157360419	A	G	51	GENIC	homozygous	112906007
4	157360747	157360748	G	C	30	GENIC	homozygous	112906009
4	157362577	157362578	T	C	46	GENIC	possibly homozygous	112906013
4	157363021	157363022	G	A	49	GENIC	homozygous	112906015
4	157363067	157363068	A	T	34	GENIC	homozygous	112906017
4	157363425	157363426	A	G	41	GENIC	homozygous	112906019
4	157364093	157364094	G	C	48	GENIC	homozygous	112906021
4	157366179	157366180	C	T	45	GENIC	homozygous	112906025
4	157366408	157366409	T	C	38	GENIC	homozygous	112906027
4	157368042	157368043	G	A	23	GENIC	homozygous	112906029
4	157368053	157368054	G	A	32	GENIC	homozygous	112906031
4	157371222	157371223	C	T	41	GENIC	homozygous	112906033
4	157371533	157371534	C	A	38	GENIC	homozygous	112906035
4	157372117	157372118	G	A	62	GENIC	possibly homozygous	112906037
4	157372818	157372819	A	G	59	GENIC	homozygous	112906039
4	157374616	157374617	A	G	16	GENIC	homozygous	112906041
4	157374714	157374715	C	G	22	GENIC	homozygous	112906043