chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	257076448	257076449	G	A	22	GENIC	homozygous	108623105
1	257077030	257077031	T	G	26	GENIC	homozygous	108623106
1	257077473	257077474	G	A	23	GENIC	homozygous	108623107
1	257077701	257077702	A	G	24	GENIC	homozygous	108623108
1	257077862	257077863	A	C	21	GENIC	homozygous	108623109
1	257078221	257078222	A	G	24	GENIC	homozygous	108623110
1	257078301	257078302	T	G	19	GENIC	homozygous	108623111
1	257078324	257078325	G	T	16	GENIC	homozygous	108623112
1	257078556	257078557	G	T	14	GENIC	homozygous	108623113
1	257078721	257078721		GTTGGAGCACAGGG	15	GENIC	homozygous	127505767
1	257078748	257078749	C	T	12	GENIC	homozygous	108623114
1	257078766	257078767	G	A	15	GENIC	homozygous	108623115
1	257078851	257078852	T	C	22	GENIC	homozygous	108623116
1	257079206	257079207	T	C	18	GENIC	homozygous	108623117
1	257079813	257079814	T	C	17	GENIC	homozygous	108623118
1	257080487	257080488	A	T	26	GENIC	homozygous	108623119
1	257080876	257080877	A	C	18	GENIC	possibly homozygous	108623121
1	257081344	257081345	G	A	15	GENIC	homozygous	108623122
1	257081669	257081670	A	T	22	GENIC	homozygous	108623123
1	257081708	257081709	A	G	27	GENIC	homozygous	108623124
1	257081709	257081710	A	C	27	GENIC	homozygous	108623125
1	257082007	257082008	T	C	13	GENIC	homozygous	108623126
1	257082334	257082335	T	C	21	GENIC	homozygous	108623127