chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	69190636	69190637	A	G	13	GENIC	homozygous	112693865
4	69190751	69190752	T	C	29	GENIC	homozygous	112693867
4	69190778	69190779	A	G	31	GENIC	homozygous	112693869
4	69191590	69191591	G	A	20	GENIC	possibly homozygous	113348015
4	69191615	69191616	C	T	22	GENIC	homozygous	113348017
4	69191950	69191951	C	T	13	GENIC	homozygous	113348019
4	69191969	69191970	A	G	13	GENIC	homozygous	112693879
4	69192155	69192156	A	T	18	GENIC	homozygous	112693883
4	69193257	69193258	G	T	12	GENIC	possibly homozygous	112693885
4	69193552	69193553	A	G	7	GENIC	homozygous	112693887
4	69193718	69193719	G	T	10	GENIC	homozygous	112693889
4	69193747	69193748	C	T	6	GENIC	homozygous	113348021
4	69194092	69194093	A	T	27	GENIC	homozygous	112693891
4	69194754	69194755	C	T	14	GENIC	homozygous	113348023
4	69195223	69195224	T	A	13	GENIC	homozygous	112693893