chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	71520804	71520805	T	-	16	GENIC	heterozygous	51490302
10	71533945	71533946	C	-	17	GENIC	homozygous	51490314
10	71533951	71533952	A	T	17	GENIC	homozygous	51490315
10	71533954	71533955	C	-	17	GENIC	homozygous	51490316
10	71534212	71534213	G	GT	16	GENIC	homozygous	51490317
10	71534219	71534220	A	AT	16	GENIC	homozygous	51490318
10	71534241	71534242	C	T	18	GENIC	homozygous	51490319
10	71534249	71534250	C	A	19	GENIC	homozygous	51490320
10	71536297	71536298	G	T	22	GENIC	homozygous	51490327
10	71536344	71536345	T	A	18	GENIC	homozygous	51490328
10	71544300	71544301	C	CCTTT	9	GENIC	heterozygous	53528989
10	71560979	71560981	CT	--	11	GENIC	heterozygous	53528990
10	71567505	71567506	G	GT	9	GENIC	heterozygous	52384315
10	71614505	71614506	A	C	11	GENIC	homozygous	51490453
10	71638174	71638175	T	TC	11	INTERGENIC	homozygous	51490525
10	71642825	71642826	A	-	13	INTERGENIC	homozygous	51490551
10	71649699	71649700	C	T	11	INTERGENIC	homozygous	51490564
10	71655392	71655394	CC	--	28	GENIC	homozygous	51490574
10	71704667	71704668	A	AT	14	GENIC	homozygous	51490654
10	71704676	71704677	A	AT	16	GENIC	homozygous	51490655
10	71713377	71713379	AC	--	7	GENIC	heterozygous	51490667
10	71719879	71719880	T	G	7	GENIC	homozygous	51490677