chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	97075330	97075331	C	T	33	GENIC	homozygous	116591232
8	97075589	97075590	A	G	18	GENIC	homozygous	116591234
8	97079004	97079005	G	T	23	GENIC	homozygous	116591238
8	97079005	97079006	A	G	23	GENIC	homozygous	116591240
8	97079506	97079507	C	T	32	GENIC	homozygous	116591242
8	97079612	97079613	G	A	28	GENIC	homozygous	116591244
8	97079873	97079874	G	A	23	GENIC	homozygous	116591246
8	97079893	97079894	G	T	24	GENIC	homozygous	116591248
8	97079933	97079934	T	C	31	GENIC	homozygous	116591250
8	97080059	97080060	C	T	40	GENIC	homozygous	116591252
8	97080088	97080089	A	G	34	GENIC	homozygous	116591254
8	97080141	97080142	A	G	35	GENIC	homozygous	116591256
8	97080182	97080183	G	A	38	GENIC	homozygous	116591258
8	97081365	97081366	A	G	29	GENIC	homozygous	116591260
8	97082799	97082800	G	C	14	GENIC	homozygous	116591262
8	97082805	97082806	A	G	13	GENIC	homozygous	116591264