chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5140768	5140769	A	G	17	GENIC	homozygous	109077201
20	5141878	5141880	CC		5	GENIC	homozygous	129653186
20	5143645	5143646	T	A	11	GENIC	homozygous	109077234
20	5147298	5147299	T	C	13	GENIC	homozygous	109077256
20	5149212	5149213	T	C	13	GENIC	homozygous	109420112
20	5149347	5149348	G	T	9	GENIC	possibly homozygous	109233876
20	5149588	5149588		TGGGGT	11	GENIC	homozygous	129653194
20	5151074	5151075	C	T	13	GENIC	homozygous	109420114
20	5151359	5151360	A	G	20	GENIC	homozygous	109077300
20	5151409	5151410	C	T	14	GENIC	homozygous	109077302
20	5152941	5152942	T	C	10	GENIC	homozygous	109077310
20	5152961	5152962	T		10	GENIC	homozygous	129653196
20	5154700	5154700		AA	10	GENIC	homozygous	129653197
20	5149296	5149299	AAT		11	GENIC	homozygous	131227939