chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	257077030	257077031	T	G	42	GENIC	homozygous	108623106
1	257077701	257077702	A	G	51	GENIC	homozygous	108623108
1	257077862	257077863	A	C	62	GENIC	homozygous	108623109
1	257078464	257078465	G		61	GENIC	homozygous	132542694
1	257078554	257078555	G		54	GENIC	homozygous	131267045
1	257078851	257078852	T	C	43	GENIC	homozygous	108623116
1	257079206	257079207	T	C	43	GENIC	homozygous	108623117
1	257079386	257079387	T	C	49	GENIC	homozygous	109024295
1	257078503	257078504	G	A	63	GENIC	homozygous	109024291
1	257078935	257078936	G	A	37	GENIC	homozygous	109024292
1	257079107	257079108	C	T	53	GENIC	homozygous	109024293
1	257079207	257079208	G	A	44	GENIC	homozygous	109024294
1	257078721	257078721		GTTGGAGCACAGGG	40	GENIC	homozygous	127505767
1	257079813	257079814	T	C	39	GENIC	homozygous	108623118
1	257080487	257080488	A	T	40	GENIC	homozygous	108623119
1	257080948	257080949	T	C	37	GENIC	homozygous	109024296
1	257081344	257081345	G	A	52	GENIC	homozygous	108623122
1	257081669	257081670	A	T	47	GENIC	homozygous	108623123
1	257081708	257081709	A	G	48	GENIC	homozygous	108623124
1	257081709	257081710	A	C	48	GENIC	homozygous	108623125
1	257082007	257082008	T	C	46	GENIC	homozygous	108623126
1	257082334	257082335	T	C	48	GENIC	homozygous	108623127