chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	67673240	67673241	T	C	20	GENIC	homozygous	114377881
13	67675261	67675261		T	17	GENIC	heterozygous	132894720
13	67675337	67675338	C	T	17	GENIC	homozygous	114631436
13	67677155	67677156	T	C	17	GENIC	homozygous	114377883
13	67678093	67678094	C	G	16	GENIC	homozygous	114377884
13	67678562	67678563	A	G	8	GENIC	homozygous	114377885
13	67679165	67679166	C	T	16	GENIC	homozygous	114377886
13	67679385	67679386	G	T	14	GENIC	homozygous	114631438
13	67679732	67679733	G	A	17	GENIC	homozygous	114377887
13	67680639	67680639		A	16	GENIC	homozygous	129067203
13	67681269	67681270	A	G	24	GENIC	homozygous	114377889
13	67681476	67681476		CATGGGGATGACGGGAAAAATCATGCACTAGTCCATCATAATGATTATATTTTTCCTGTTTCGTGTGAACTTAGGTCACACAATGC	14	GENIC	homozygous	129067204
13	67681518	67681519	G	A	18	GENIC	homozygous	114631440
13	67681756	67681757	C	T	18	GENIC	homozygous	114377890
13	67682583	67682583		T	17	GENIC	possibly homozygous	129067205
13	67682729	67682730	A	G	15	GENIC	homozygous	114377891
13	67682758	67682759	T		16	GENIC	homozygous	129067206
13	67683376	67683377	A	G	16	GENIC	homozygous	114377892
13	67686607	67686608	C	G	23	GENIC	homozygous	114631442
13	67686662	67686664	TG		24	GENIC	homozygous	129067207
13	67687241	67687242	A	C	25	GENIC	homozygous	114377894
13	67687381	67687382	C	T	13	GENIC	homozygous	114377895
13	67688184	67688185	T		12	GENIC	possibly homozygous	129067208
13	67688691	67688692	A		13	GENIC	homozygous	129067209