chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	27733770	27733771	T	C	40	GENIC	homozygous	110455609
18	27735459	27735460	T	C	42	GENIC	homozygous	110455611
18	27735918	27735919	G	A	42	GENIC	homozygous	110455612
18	27735983	27735984	G	C	35	GENIC	homozygous	110455613
18	27737340	27737341	T	C	34	GENIC	homozygous	110455614
18	27738267	27738268	G	C	41	GENIC	homozygous	110455615
18	27738755	27738756	A	G	30	GENIC	homozygous	110455616
18	27740535	27740536	C	T	45	GENIC	homozygous	110455617
18	27740911	27740912	T	C	49	GENIC	homozygous	110455618
18	27742821	27742822	A	G	44	GENIC	homozygous	110649236
18	27743516	27743517	A	G	32	GENIC	homozygous	110455619
18	27743644	27743645	T	A	38	GENIC	homozygous	110455620
18	27744718	27744719	G	T	32	GENIC	homozygous	110649237
18	27745875	27745876	C	T	30	GENIC	homozygous	110455621
18	27746309	27746310	T	C	33	GENIC	homozygous	110455622
18	27746659	27746660	T	C	35	GENIC	homozygous	110455623
18	27748273	27748274	T	C	30	GENIC	homozygous	110649238
18	27748371	27748372	C	T	24	GENIC	homozygous	110455625