chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	54108626	54108627	C	T	19	GENIC	homozygous	110355336
18	54109043	54109044	C	T	27	GENIC	homozygous	110355339
18	54109457	54109458	G	A	19	GENIC	homozygous	110355343
18	54110332	54110333	A	T	26	GENIC	homozygous	110538661
18	54110521	54110522	A	G	26	GENIC	homozygous	110654447
18	54110634	54110635	A	G	20	GENIC	homozygous	110538665
18	54110714	54110715	A	G	24	GENIC	homozygous	110538667
18	54111559	54111560	G	A	20	GENIC	homozygous	110654448
18	54112192	54112193	A	G	40	GENIC	homozygous	110731848
18	54112747	54112748	T	G	10	GENIC	homozygous	110538669
18	54112763	54112764	T	C	7	GENIC	homozygous	110355347
18	54112975	54112976	A	G	19	GENIC	homozygous	110355349
18	54113394	54113395	A	G	19	GENIC	homozygous	110538671
18	54113480	54113481	T	C	13	GENIC	homozygous	110538673
18	54114134	54114135	G	A	27	GENIC	homozygous	110538675
18	54116178	54116179	C	G	20	GENIC	homozygous	110355355
18	54117303	54117304	T	G	34	GENIC	homozygous	110355359
18	54118320	54118321	A	G	32	GENIC	homozygous	110355361
18	54118489	54118490	C	T	13	GENIC	homozygous	110654450
18	54118588	54118589	C	T	16	GENIC	homozygous	110355363
18	54118801	54118802	G	T	35	GENIC	homozygous	110355365
18	54119308	54119309	A	G	22	GENIC	homozygous	110355367
18	54122705	54122706	A	G	14	GENIC	homozygous	110355371