chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157791822	157791823	T	C	27	GENIC	homozygous	112907272
4	157791833	157791834	T	C	23	GENIC	homozygous	112907274
4	157791845	157791846	T	A	22	GENIC	possibly homozygous	112907276
4	157791851	157791852	T	C	25	GENIC	heterozygous	112907278
4	157791863	157791864	A	T	25	GENIC	heterozygous	112907280
4	157792271	157792272	G	A	30	GENIC	homozygous	112907282
4	157793017	157793018	G	T	28	GENIC	possibly homozygous	112907284
4	157795166	157795167	C	T	27	GENIC	homozygous	112907286
4	157796662	157796663	T	C	20	GENIC	homozygous	112907288
4	157796750	157796751	C	T	25	GENIC	homozygous	112907290
4	157797124	157797125	G	A	39	GENIC	homozygous	112907292
4	157797798	157797799	G	T	23	GENIC	heterozygous	112907294
4	157797801	157797802	C	T	23	GENIC	heterozygous	112907296
4	157797854	157797855	T	G	25	GENIC	possibly homozygous	112907298
4	157798356	157798357	T	G	29	GENIC	homozygous	112907300