chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	109624306	109624307	G	T	53	INTERGENIC	homozygous	114443230
13	109625040	109625041	A	G	43	INTERGENIC	possibly homozygous	114443232
13	109625388	109625389	T	C	66	INTERGENIC	possibly homozygous	114443234
13	109625449	109625450	C	G	67	INTERGENIC	possibly homozygous	114443236
13	109626131	109626132	T	A	31	INTERGENIC	homozygous	114726210
13	109626204	109626205	A	G	48	INTERGENIC	homozygous	114443238
13	109626344	109626345	C	A	57	INTERGENIC	homozygous	114443240
13	109626908	109626909	G	A	72	INTERGENIC	possibly homozygous	114443242
13	109626950	109626951	G	A	55	INTERGENIC	possibly homozygous	114443244
13	109627237	109627238	A	T	50	INTERGENIC	homozygous	118468588
13	109627444	109627445	C	T	64	INTERGENIC	possibly homozygous	114443246
13	109627449	109627450	T	C	62	INTERGENIC	possibly homozygous	114443248
13	109627787	109627788	T	G	59	INTERGENIC	homozygous	114443250
13	109627867	109627868	G	C	56	INTERGENIC	homozygous	114443252
13	109628295	109628296	A	G	73	INTERGENIC	homozygous	114443254
13	109628686	109628687	A	G	64	INTERGENIC	homozygous	114443256
13	109628796	109628797	C	G	51	INTERGENIC	possibly homozygous	114443258
13	109629226	109629227	G	C	30	INTERGENIC	homozygous	114443260
13	109629316	109629317	C	G	32	INTERGENIC	homozygous	114443262