chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	111248726	111248727	A	AAAAGG	3	GENIC	homozygous	52806297
8	111249550	111249551	A	G	11	GENIC	homozygous	52806303
8	111249980	111249981	C	CA	20	GENIC	homozygous	52806309
8	111250038	111250039	A	G	18	GENIC	homozygous	52806312
8	111250068	111250069	A	G	17	GENIC	possibly homozygous	52806315
8	111250231	111250232	C	T	13	GENIC	possibly homozygous	52806318
8	111250316	111250317	A	G	25	GENIC	homozygous	52806321
8	111250465	111250466	C	CA	2	GENIC	heterozygous	52806324
8	111250472	111250473	C	A	1	GENIC	homozygous	52806327
8	111250541	111250542	A	C	17	GENIC	homozygous	52806332
8	111250973	111250974	A	G	14	GENIC	homozygous	52806334
8	111251034	111251035	C	T	17	GENIC	possibly homozygous	52806337
8	111251156	111251157	T	A	24	GENIC	homozygous	52806340
8	111251320	111251321	A	C	16	GENIC	possibly homozygous	52806343
8	111251430	111251431	G	C	9	GENIC	homozygous	52806346
8	111251439	111251440	C	T	9	GENIC	homozygous	52806349
8	111251607	111251608	C	T	24	GENIC	possibly homozygous	52806352
8	111251891	111251892	A	T	11	GENIC	homozygous	52806355
8	111252043	111252044	T	C	16	GENIC	homozygous	52806358
8	111252101	111252102	A	C	21	GENIC	homozygous	52806361
8	111252158	111252159	T	C	21	GENIC	homozygous	52806364
8	111252428	111252429	G	A	19	GENIC	possibly homozygous	52806367
8	111253132	111253133	G	GGCT	7	GENIC	homozygous	52806370
8	111253681	111253682	G	A	11	GENIC	possibly homozygous	52806372
8	111253974	111253975	G	T	25	GENIC	possibly homozygous	52806375
8	111254517	111254518	C	T	19	GENIC	homozygous	52806378
8	111255083	111255084	A	G	25	GENIC	homozygous	52806381
8	111255426	111255427	A	T	20	GENIC	possibly homozygous	52806383