chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	46063509	46063510	T	C	14	GENIC	homozygous	109212053
20	46063514	46063515	C	A	13	GENIC	homozygous	109465377
20	46093401	46093402	T	G	29	GENIC	homozygous	109212057
20	46093402	46093403	G	T	29	GENIC	homozygous	109212059
20	46094467	46094468	A	T	34	GENIC	homozygous	109212061
20	46094477	46094478	C	A	35	GENIC	homozygous	109212063
20	46094479	46094480	C	T	36	GENIC	homozygous	109212065
20	46094501	46094502	T	A	41	GENIC	homozygous	109212067
20	46094534	46094535	C	G	37	GENIC	homozygous	109212070
20	46094549	46094550	A	T	34	GENIC	homozygous	109212072
20	46094590	46094591	T	A	31	GENIC	homozygous	109212074
20	46108247	46108248	A	G	32	GENIC	homozygous	109465378
20	46108328	46108329	A	C	22	GENIC	homozygous	109212076
20	46130285	46130286	A	C	18	GENIC	homozygous	109467437
20	46158036	46158037	T	G	29	GENIC	homozygous	109212080
20	46158037	46158038	G	T	27	GENIC	homozygous	109276389
20	46158039	46158040	C	G	27	GENIC	homozygous	109276391