chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	257396511	257396512	G	A	28	GENIC	homozygous	111043650
2	257398404	257398405	C	G	19	GENIC	homozygous	110411893
2	257399081	257399082	A		23	GENIC	homozygous	127768530
2	257401135	257401136	C	T	16	GENIC	homozygous	111043654
2	257401875	257401876	T	A	31	GENIC	homozygous	110411897
2	257403118	257403119	T		16	GENIC	homozygous	127768532
2	257403334	257403334		TGTGT	12	GENIC	homozygous	132022216
2	257403607	257403608	A	G	23	GENIC	homozygous	110411899
2	257404394	257404395	T	C	18	GENIC	homozygous	110411901
2	257406828	257406829	G	A	33	GENIC	homozygous	111043656
2	257407718	257407719	C	T	29	GENIC	homozygous	110411909
2	257407770	257407771	G	A	15	GENIC	homozygous	111043658
2	257408313	257408314	G	A	11	GENIC	homozygous	111043660
2	257408979	257408980	G	A	18	GENIC	homozygous	111043662
2	257411008	257411009	G	A	27	GENIC	homozygous	111043664
2	257413888	257413889	G	A	28	GENIC	homozygous	111043666
2	257415716	257415717	T	C	26	GENIC	homozygous	110411923
2	257403335	257403335		G	11	GENIC	homozygous	132022217
2	257408329	257408365	TCTAGCCTGCCGTAGCGTGCAGTCAGTCGCTCAGGA		7	GENIC	homozygous	131304652
2	257416115	257416116	A	G	23	GENIC	homozygous	111043668
2	257423916	257423917	C	T	24	GENIC	homozygous	111043670