chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	130120530	130120531	A	G	35	GENIC	homozygous	116724660
8	130120581	130120582	G	A	32	GENIC	homozygous	116724661
8	130120680	130120681	G	T	31	GENIC	homozygous	116724662
8	130120697	130120698	C	A	34	GENIC	homozygous	116724663
8	130120847	130120848	A	G	31	GENIC	homozygous	116724664
8	130121116	130121117	C	G	31	GENIC	homozygous	116724665
8	130121305	130121306	G	T	21	GENIC	homozygous	116724666
8	130122325	130122326	A	G	32	GENIC	homozygous	116724668
8	130122465	130122466	C	T	20	GENIC	homozygous	116724669
8	130122957	130122958	C	A	20	GENIC	homozygous	116724670
8	130123073	130123074	A	G	27	GENIC	homozygous	116724671
8	130123309	130123310	G	A	35	GENIC	homozygous	116724672
8	130123529	130123530	G	A	24	GENIC	homozygous	116724673
8	130123547	130123548	C	T	26	GENIC	homozygous	116724674
8	130124110	130124111	T	C	22	GENIC	homozygous	116724675
8	130124162	130124163	A	C	27	GENIC	homozygous	116724676
8	130124720	130124721	A	T	23	GENIC	homozygous	116724678
8	130124734	130124735	T	C	23	GENIC	homozygous	116724679
8	130125544	130125545	G	A	36	GENIC	homozygous	116724680
8	130126053	130126054	C	G	32	GENIC	homozygous	116724681
8	130127107	130127108	T	G	21	GENIC	homozygous	116724682
8	130127420	130127421	G	A	25	GENIC	homozygous	116724683