chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	82739243	82739244	T	G	38	GENIC	homozygous	114411855
13	82739791	82739792	A	G	36	GENIC	homozygous	114411857
13	82741514	82741515	A	T	30	GENIC	homozygous	114567273
13	82741557	82741558	C	T	39	GENIC	homozygous	114567274
13	82741837	82741838	A	G	34	GENIC	homozygous	114411859
13	82741860	82741861	A	G	31	GENIC	homozygous	114567275
13	82742263	82742264	C	T	27	GENIC	homozygous	114567276
13	82742328	82742329	C	T	33	GENIC	homozygous	114567277
13	82742914	82742915	C	T	26	GENIC	homozygous	114567278
13	82743600	82743601	T	C	41	GENIC	homozygous	114411861
13	82743607	82743608	T	A	39	GENIC	homozygous	114411863
13	82746336	82746337	T	C	37	GENIC	homozygous	114567279
13	82747288	82747289	A	G	39	GENIC	homozygous	114567280
13	82747814	82747815	A	G	33	GENIC	homozygous	114411867
13	82748417	82748418	T	C	34	GENIC	homozygous	114567281
13	82750284	82750285	T	A	39	GENIC	homozygous	114567282
13	82751114	82751115	A	T	36	GENIC	homozygous	114567283
13	82751191	82751192	T	C	32	GENIC	homozygous	114567284
13	82751318	82751319	T	G	33	GENIC	homozygous	114411875
13	82751341	82751342	A	G	31	GENIC	homozygous	114411877
13	82752576	82752577	C	T	40	GENIC	homozygous	114567285
13	82753708	82753709	A	C	29	GENIC	homozygous	114411887