chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	23491929	23491930	A	G	31	GENIC	homozygous	117909640
8	23499028	23499029	T	C	21	GENIC	homozygous	116440183
8	23568055	23568056	A	T	6	GENIC	homozygous	116440208
8	23712423	23712424	G	C	26	GENIC	homozygous	116440216
8	23712424	23712425	G	C	26	GENIC	homozygous	116440217
8	23718740	23718741	A	T	21	GENIC	homozygous	116440232
8	23719311	23719312	T	G	17	GENIC	homozygous	118089595
8	23719313	23719314	T	G	17	GENIC	homozygous	118089597
8	23719314	23719315	G	T	16	GENIC	homozygous	117932012
8	23719466	23719467	A	G	14	GENIC	homozygous	118015455
8	23719504	23719505	A	T	23	GENIC	homozygous	117909644
8	23719505	23719506	G	A	23	GENIC	homozygous	117909645
8	23719547	23719548	A	T	24	GENIC	homozygous	116440235
8	23719852	23719853	A	G	18	GENIC	homozygous	116779275
8	23718854	23718855	A	T	22	GENIC	homozygous	118117252
8	23876027	23876028	A	G	45	GENIC	homozygous	116440273
8	23877587	23877588	G	T	28	GENIC	homozygous	116440274
8	23877592	23877593	A	T	25	GENIC	homozygous	117909649
8	23877600	23877601	G	A	27	GENIC	homozygous	117909650
8	23877601	23877602	A	G	26	GENIC	homozygous	117909651