chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	127905678	127905679	C	T	21	GENIC	homozygous	116719726
8	127906112	127906113	A	G	17	GENIC	homozygous	116719728
8	127909379	127909380	A	G	11	GENIC	homozygous	116719730
8	127909693	127909694	C	G	5	GENIC	homozygous	116989737
8	127910804	127910805	C	T	2	GENIC	homozygous	116719732
8	127912620	127912621	C	T	30	GENIC	homozygous	116719734
8	127913624	127913625	T	C	30	GENIC	homozygous	116719736
8	127913961	127913962	A	G	24	GENIC	homozygous	116719738
8	127914078	127914079	A	G	17	GENIC	homozygous	116719780
8	127909146	127909146		G	11	GENIC	homozygous	128646813
8	127911594	127911601	GCCCGCT		3	GENIC	homozygous	132126068
8	127913045	127913046	C		25	GENIC	homozygous	128646815
8	127909480	127909481	G	T	21	GENIC	homozygous	128668476
8	127909482	127909483	C	G	21	GENIC	homozygous	128668477
8	127909489	127909490	G	A	21	GENIC	homozygous	128668478
8	127910200	127910201	G	A	4	GENIC	homozygous	128668479
8	127910253	127910254	C	T	8	GENIC	homozygous	128668480
8	127910140	127910141	C	T	3	GENIC	homozygous	117176076
8	127914885	127914886	T	A	21	GENIC	homozygous	117006850