chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	25342997	25342998	G	A	17	GENIC	homozygous	115792315
11	25343093	25343094	C	T	20	GENIC	homozygous	115792317
11	25343188	25343189	A	C	17	GENIC	homozygous	115792319
11	25343829	25343830	C	T	20	GENIC	homozygous	115792321
11	25344345	25344346	T	C	23	GENIC	homozygous	115792323
11	25345554	25345555	A	G	28	GENIC	homozygous	115792325
11	25346560	25346560		GA	2	GENIC	homozygous	128892235
11	25347639	25347640	A	G	25	GENIC	homozygous	115792327
11	25349005	25349006	T	G	24	GENIC	homozygous	115792329
11	25349195	25349196	A	T	21	GENIC	homozygous	115792331
11	25349609	25349610	T	C	20	GENIC	homozygous	115792333
11	25350334	25350335	C	T	23	GENIC	homozygous	115792335
11	25350417	25350418	T	C	23	GENIC	homozygous	115792337
11	25350594	25350594		GGTTAGAC	20	GENIC	homozygous	128892236
11	25350737	25350737		T	18	GENIC	homozygous	128892237
11	25350756	25350759	AGT		19	GENIC	homozygous	128892238
11	25350785	25350786	C	T	21	GENIC	homozygous	115792339