chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	67673240	67673241	T	C	48	GENIC	homozygous	114377881
13	67673909	67673910	T	C	50	GENIC	homozygous	114377882
13	67674086	67674086		ATT	56	GENIC	homozygous	129067202
13	67677155	67677156	T	C	43	GENIC	homozygous	114377883
13	67678093	67678094	C	G	33	GENIC	homozygous	114377884
13	67678562	67678563	A	G	46	GENIC	homozygous	114377885
13	67679165	67679166	C	T	42	GENIC	homozygous	114377886
13	67679732	67679733	G	A	46	GENIC	homozygous	114377887
13	67680420	67680421	A	G	49	GENIC	homozygous	114377888
13	67680639	67680639		A	39	GENIC	homozygous	129067203
13	67681269	67681270	A	G	60	GENIC	homozygous	114377889
13	67681476	67681476		CATGGGGATGACGGGAAAAATCATGCACTAGTCCATCATAATGATTATATTTTTCCTGTTTCGTGTGAACTTAGGTCACACAATGC	39	GENIC	homozygous	129067204
13	67681756	67681757	C	T	54	GENIC	homozygous	114377890
13	67682583	67682583		T	40	GENIC	possibly homozygous	129067205
13	67682729	67682730	A	G	51	GENIC	homozygous	114377891
13	67682758	67682759	T		50	GENIC	homozygous	129067206
13	67683376	67683377	A	G	51	GENIC	homozygous	114377892
13	67686044	67686045	T	C	38	GENIC	homozygous	114377893
13	67686662	67686664	TG		36	GENIC	homozygous	129067207
13	67687241	67687242	A	C	49	GENIC	homozygous	114377894
13	67687381	67687382	C	T	42	GENIC	homozygous	114377895
13	67688184	67688185	T		37	GENIC	possibly homozygous	129067208
13	67688691	67688692	A		41	GENIC	possibly homozygous	129067209