chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	61638496	61638497	T	C	27	GENIC	homozygous	110372321
18	61638706	61638707	T	C	27	GENIC	homozygous	110372323
18	61638708	61638709	G	A	27	GENIC	homozygous	110372325
18	61638814	61638815	C	T	33	GENIC	homozygous	110372327
18	61638868	61638869	G	A	32	GENIC	homozygous	110372329
18	61638884	61638885	G	A	31	GENIC	homozygous	110372331
18	61638996	61638997	T	C	25	GENIC	homozygous	110372333
18	61639039	61639040	G	T	28	GENIC	homozygous	110372335
18	61639077	61639078	C	T	30	GENIC	homozygous	110372337
18	61639184	61639185	G	A	24	GENIC	homozygous	110372339
18	61639309	61639310	T	C	29	GENIC	homozygous	110372341
18	61639447	61639448	C	T	22	GENIC	homozygous	110372343
18	61639475	61639476	T	C	22	GENIC	homozygous	110372345
18	61639651	61639652	C	T	16	GENIC	homozygous	110372347
18	61639660	61639661	C	T	17	GENIC	homozygous	110372349
18	61639868	61639869	A	T	28	GENIC	homozygous	110372351
18	61640035	61640036	T	C	23	GENIC	homozygous	110372353
18	61640106	61640107	A	G	30	GENIC	homozygous	110372355
18	61640197	61640198	A	G	23	GENIC	homozygous	110372357
18	61640307	61640308	C	T	21	GENIC	homozygous	110372359
18	61640393	61640394	G	A	31	GENIC	homozygous	110372361
18	61640566	61640567	T	G	26	GENIC	homozygous	110372363
18	61640616	61640617	T	C	26	GENIC	homozygous	110372365
18	61640620	61640621	T	C	27	GENIC	homozygous	110372367