chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	40410728	40410729	T	C	31	GENIC	homozygous	116802814
8	40410975	40410976	T	C	28	GENIC	homozygous	116802816
8	40411060	40411061	C	T	40	GENIC	homozygous	116802819
8	40411281	40411282	C	T	45	GENIC	homozygous	116802821
8	40411389	40411390	G	A	37	GENIC	homozygous	116802823
8	40411444	40411445	C	A	35	GENIC	homozygous	116802825
8	40411598	40411599	T	A	28	GENIC	homozygous	116802827
8	40411738	40411739	T	C	21	GENIC	homozygous	116802829
8	40411764	40411765	G	T	18	GENIC	homozygous	116802831
8	40412035	40412036	A	C	15	GENIC	homozygous	116802833
8	40412662	40412663	G	A	16	GENIC	homozygous	116802837
8	40412725	40412726	G	A	21	GENIC	homozygous	116802839
8	40412872	40412873	A	G	11	GENIC	homozygous	116802841
8	40413359	40413360	A	G	22	GENIC	homozygous	116802843
8	40413512	40413513	G	C	26	GENIC	homozygous	116802845
8	40413946	40413947	A	G	23	GENIC	homozygous	116802851
8	40414012	40414013	G	C	22	GENIC	homozygous	116802853