chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	8809211	8809212	T	C	12	GENIC	homozygous	50036222
12	8809267	8809268	A	G	16	GENIC	homozygous	50036228
12	8815869	8815870	T	C	14	GENIC	homozygous	50036237
12	8815932	8815933	G	A	15	GENIC	homozygous	50036239
12	8815968	8815969	C	G	16	GENIC	homozygous	50036241
12	8816043	8816044	T	C	10	GENIC	homozygous	50036243
12	8816053	8816054	A	G	10	GENIC	homozygous	50036245
12	8816102	8816103	G	A	12	GENIC	homozygous	50036247
12	8816180	8816181	C	CACTT	19	GENIC	homozygous	50036249
12	8816332	8816333	A	G	14	GENIC	homozygous	50036251
12	8816362	8816363	C	T	16	GENIC	homozygous	50036253
12	8816408	8816409	G	A	15	GENIC	homozygous	50036255
12	8816410	8816413	CTT	---	15	GENIC	homozygous	50036257
12	8816415	8816416	T	A	15	GENIC	homozygous	50036259
12	8816435	8816436	C	T	17	GENIC	homozygous	50036261
12	8818343	8818344	A	AT	7	GENIC	homozygous	50036267
12	8821007	8821008	C	G	13	GENIC	homozygous	51087969