chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	40180327	40180328	G	A	29	GENIC	homozygous	110329054
18	40180560	40180561	C	T	17	GENIC	homozygous	110329056
18	40186543	40186544	T	C	24	GENIC	homozygous	110329058
18	40189384	40189385	A	G	19	GENIC	homozygous	110329060
18	40191521	40191522	A	G	18	GENIC	homozygous	110329062
18	40192882	40192883	T	C	9	GENIC	homozygous	110329064
18	40193271	40193272	C	T	23	GENIC	homozygous	110533319
18	40194326	40194327	T	C	13	GENIC	homozygous	110329066
18	40195857	40195858	C	A	13	GENIC	homozygous	110329068
18	40196834	40196835	C	T	11	GENIC	homozygous	110533325
18	40198069	40198070	G	T	17	GENIC	homozygous	110630560
18	40199024	40199025	A	G	21	GENIC	homozygous	110329072
18	40202432	40202433	A	T	13	GENIC	homozygous	110329074
18	40202692	40202693	C	T	13	GENIC	homozygous	110329076
18	40203703	40203704	A	C	17	GENIC	homozygous	110329078
18	40205432	40205433	A	G	30	GENIC	homozygous	110329080
18	40206106	40206107	T	C	19	GENIC	homozygous	110329082
18	40209763	40209764	C	T	18	GENIC	homozygous	110329084
18	40209948	40209949	C	T	25	GENIC	homozygous	110329086
18	40210420	40210421	T	C	25	GENIC	homozygous	110329088
18	40212317	40212318	T	C	20	GENIC	homozygous	110329090
18	40212343	40212344	G	A	25	GENIC	homozygous	110329092
18	40215187	40215188	T	C	23	GENIC	homozygous	110329094
18	40217054	40217055	A	G	15	GENIC	homozygous	110329096