chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	82739243	82739244	T	G	36	GENIC	homozygous	114411855
13	82739791	82739792	A	G	42	GENIC	homozygous	114411857
13	82740958	82740959	C	T	21	GENIC	homozygous	114692134
13	82741837	82741838	A	G	19	GENIC	homozygous	114411859
13	82741860	82741861	A	G	15	GENIC	homozygous	114567275
13	82742241	82742242	A	T	27	GENIC	homozygous	114692135
13	82742792	82742793	G	A	29	GENIC	homozygous	114692136
13	82742910	82742911	G	C	21	GENIC	homozygous	114692137
13	82742914	82742915	C	T	21	GENIC	homozygous	114567278
13	82743228	82743229	C	T	22	GENIC	homozygous	114692139
13	82743559	82743560	G	A	27	GENIC	homozygous	115120966
13	82743600	82743601	T	C	37	GENIC	homozygous	114411861
13	82743607	82743608	T	A	34	GENIC	homozygous	114411863
13	82743844	82743845	G	A	37	GENIC	homozygous	114692140
13	82743988	82743989	G	A	40	GENIC	homozygous	114692141
13	82744550	82744551	A	G	19	GENIC	homozygous	114692143
13	82744942	82744943	G	A	39	GENIC	homozygous	114692144
13	82746336	82746337	T	C	25	GENIC	homozygous	114567279
13	82750284	82750285	T	A	34	GENIC	homozygous	114567282
13	82747288	82747289	A	G	38	GENIC	possibly homozygous	114567280
13	82747524	82747525	A	G	21	GENIC	homozygous	114692145
13	82747814	82747815	A	G	35	GENIC	homozygous	114411867
13	82749052	82749053	T	C	24	GENIC	homozygous	114692146
13	82751318	82751319	T	G	25	GENIC	homozygous	114411875
13	82751341	82751342	A	G	27	GENIC	homozygous	114411877
13	82751746	82751747	A	T	9	GENIC	homozygous	114411881
13	82752282	82752283	G	T	35	GENIC	homozygous	115120972
13	82752697	82752698	C	T	14	GENIC	homozygous	114411883
13	82752698	82752699	C	T	14	GENIC	homozygous	114411885
13	82752806	82752807	T	C	10	GENIC	homozygous	115120974
13	82753647	82753648	C	A	42	GENIC	homozygous	115120976
13	82753708	82753709	A	C	29	GENIC	homozygous	114411887
13	82753871	82753872	G	A	18	GENIC	homozygous	114411889