chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157359381	157359382	T	C	57	GENIC	homozygous	112905999
4	157359635	157359636	A	T	47	GENIC	homozygous	112906001
4	157359881	157359882	G	T	64	GENIC	homozygous	112906003
4	157359944	157359945	G	A	72	GENIC	homozygous	112906005
4	157360418	157360419	A	G	80	GENIC	homozygous	112906007
4	157360747	157360748	G	C	68	GENIC	homozygous	112906009
4	157361990	157361990		GTTTTGTTTTGTTTTG	41	GENIC	homozygous	128096095
4	157362088	157362089	C	T	38	GENIC	homozygous	112906011
4	157362577	157362578	T	C	52	GENIC	homozygous	112906013
4	157362785	157362785		G	47	GENIC	homozygous	128096096
4	157363021	157363022	G	A	54	GENIC	homozygous	112906015
4	157363067	157363068	A	T	53	GENIC	homozygous	112906017
4	157363425	157363426	A	G	49	GENIC	homozygous	112906019
4	157364093	157364094	G	C	63	GENIC	homozygous	112906021
4	157366062	157366063	G	A	49	GENIC	homozygous	112906023
4	157366179	157366180	C	T	46	GENIC	homozygous	112906025
4	157366262	157366265	TCC		44	GENIC	homozygous	128096097
4	157366408	157366409	T	C	51	GENIC	homozygous	112906027
4	157368053	157368054	G	A	41	GENIC	homozygous	112906031
4	157370575	157370575		TGA	41	GENIC	homozygous	128096098
4	157371222	157371223	C	T	52	GENIC	homozygous	112906033
4	157371533	157371534	C	A	47	GENIC	possibly homozygous	112906035
4	157372117	157372118	G	A	52	GENIC	homozygous	112906037
4	157372818	157372819	A	G	54	GENIC	homozygous	112906039
4	157373711	157373719	TCTCTGTC		30	GENIC	homozygous	128096099
4	157374616	157374617	A	G	48	GENIC	homozygous	112906041
4	157374714	157374715	C	G	34	GENIC	possibly homozygous	112906043