chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	257077030	257077031	T	G	34	GENIC	homozygous	108623106
1	257077701	257077702	A	G	17	GENIC	homozygous	108623108
1	257077862	257077863	A	C	15	GENIC	homozygous	108623109
1	257078503	257078504	G	A	30	GENIC	homozygous	109024291
1	257078554	257078555	G		23	GENIC	homozygous	131267045
1	257078721	257078721		GTTGGAGCACAGGG	18	GENIC	homozygous	127505767
1	257078851	257078852	T	C	23	GENIC	homozygous	108623116
1	257079206	257079207	T	C	20	GENIC	homozygous	108623117
1	257079207	257079208	G	A	20	GENIC	homozygous	109024294
1	257079813	257079814	T	C	14	GENIC	homozygous	108623118
1	257080081	257080082	G	A	27	GENIC	homozygous	109215323
1	257080487	257080488	A	T	28	GENIC	homozygous	108623119
1	257080948	257080949	T	C	22	GENIC	homozygous	109024296
1	257081065	257081066	G	A	17	GENIC	homozygous	109215325
1	257081344	257081345	G	A	21	GENIC	homozygous	108623122
1	257081476	257081477	A	T	22	GENIC	homozygous	109215327
1	257081669	257081670	A	T	14	GENIC	homozygous	108623123
1	257081708	257081709	A	G	15	GENIC	homozygous	108623124
1	257081709	257081710	A	C	15	GENIC	homozygous	108623125
1	257082007	257082008	T	C	17	GENIC	homozygous	108623126
1	257082334	257082335	T	C	16	GENIC	homozygous	108623127
1	257082385	257082386	A	G	14	GENIC	homozygous	109215329