chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	40178794	40178795	A	T	43	GENIC	heterozygous	119490539
18	40180327	40180328	G	A	44	GENIC	homozygous	110329054
18	40180560	40180561	C	T	35	GENIC	homozygous	110329056
18	40186543	40186544	T	C	62	GENIC	homozygous	110329058
18	40187848	40187849	C	A	22	GENIC	heterozygous	119490540
18	40189384	40189385	A	G	31	GENIC	homozygous	110329060
18	40189924	40189925	C	T	26	GENIC	homozygous	110533317
18	40191521	40191522	A	G	44	GENIC	homozygous	110329062
18	40192882	40192883	T	C	18	GENIC	homozygous	110329064
18	40193271	40193272	C	T	60	GENIC	possibly homozygous	110533319
18	40194326	40194327	T	C	29	GENIC	homozygous	110329066
18	40194749	40194750	C	T	32	GENIC	homozygous	110533321
18	40195857	40195858	C	A	27	GENIC	possibly homozygous	110329068
18	40196427	40196428	A	G	46	GENIC	possibly homozygous	110533323
18	40196834	40196835	C	T	28	GENIC	possibly homozygous	110533325
18	40197102	40197103	C	A	41	GENIC	possibly homozygous	119490541
18	40197651	40197652	A	G	44	GENIC	homozygous	119490542
18	40197774	40197775	G	T	80	GENIC	heterozygous	119490543
18	40197776	40197777	C	T	81	GENIC	heterozygous	119490544
18	40198069	40198070	G	T	39	GENIC	homozygous	110630560
18	40198869	40198870	G	T	28	GENIC	possibly homozygous	110329070
18	40199024	40199025	A	G	21	GENIC	homozygous	110329072
18	40202432	40202433	A	T	34	GENIC	homozygous	110329074
18	40202692	40202693	C	T	15	GENIC	homozygous	110329076
18	40203703	40203704	A	C	34	GENIC	homozygous	110329078
18	40205432	40205433	A	G	38	GENIC	homozygous	110329080
18	40206106	40206107	T	C	45	GENIC	homozygous	110329082
18	40209763	40209764	C	T	39	GENIC	homozygous	110329084
18	40209948	40209949	C	T	43	GENIC	homozygous	110329086
18	40210420	40210421	T	C	39	GENIC	homozygous	110329088
18	40212317	40212318	T	C	55	GENIC	homozygous	110329090
18	40212343	40212344	G	A	53	GENIC	homozygous	110329092
18	40215187	40215188	T	C	25	GENIC	homozygous	110329094
18	40217054	40217055	A	G	14	GENIC	homozygous	110329096