chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	281066400	281066401	G	A	24	GENIC	homozygous	108669326
1	281066783	281066784	C	T	28	GENIC	homozygous	108669327
1	281067900	281067901	G	A	15	GENIC	homozygous	108669328
1	281068938	281068939	A	G	9	GENIC	homozygous	108669329
1	281069137	281069138	T	C	6	GENIC	homozygous	108669330
1	281071635	281071636	C	T	11	GENIC	homozygous	108669331
1	281072910	281072911	C	A	34	GENIC	homozygous	108669332
1	281073051	281073052	A	C	41	GENIC	homozygous	108669333
1	281073112	281073113	C	T	39	GENIC	homozygous	108669334
1	281074099	281074100	T	A	28	GENIC	homozygous	108669335
1	281074239	281074240	A	G	32	GENIC	homozygous	108669336
1	281074948	281074949	T	C	27	GENIC	homozygous	108669337
1	281076716	281076717	T	C	25	GENIC	homozygous	108669338
1	281079975	281079976	C	T	17	GENIC	homozygous	108669339
1	281080337	281080338	T	C	27	GENIC	homozygous	108669340
1	281081528	281081529	T	C	21	GENIC	homozygous	108669341
1	281083336	281083337	G	A	8	GENIC	homozygous	108669342
1	281083372	281083373	C	T	14	GENIC	homozygous	108669343
1	281083424	281083425	C	T	15	GENIC	homozygous	108669344
1	281085991	281085992	T	C	31	GENIC	homozygous	108669345
1	281086118	281086119	T	C	34	GENIC	homozygous	108669346
1	281086540	281086541	C	T	31	GENIC	homozygous	108669347
1	281087981	281087982	C	A	16	GENIC	homozygous	108669349
1	281088091	281088092	C	A	19	GENIC	homozygous	108669350
1	281088652	281088653	G	A	38	GENIC	homozygous	108669351
1	281088756	281088757	G	A	28	GENIC	homozygous	108669352
1	281090301	281090302	T	C	29	GENIC	homozygous	108669353
1	281090501	281090502	A	G	26	GENIC	homozygous	108669354
1	281092719	281092720	A	G	22	GENIC	homozygous	108669357
1	281094672	281094673	A	G	20	GENIC	homozygous	108669358
1	281095950	281095951	C	A	3	GENIC	homozygous	108669360
1	281097018	281097019	C	A	26	GENIC	homozygous	108669361
1	281097340	281097341	A	T	30	GENIC	homozygous	108669362
1	281097811	281097812	T	G	16	GENIC	homozygous	108669363
1	281100536	281100537	A	T	4	GENIC	homozygous	108669364