chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	61713775	61713781	CTGGGA	------	24	GENIC	homozygous	53636105
8	61713782	61713783	T	TCCA	25	GENIC	homozygous	53646617
8	61713783	61713784	G	GAA	25	GENIC	homozygous	53646618
8	61713900	61713901	A	G	36	GENIC	homozygous	53636106
8	61713924	61713925	G	T	25	GENIC	homozygous	53636107
8	61713986	61713987	G	GTGTGTGTGTGTGTGTGTA	13	GENIC	possibly homozygous	53636108
8	61714130	61714131	T	TGTGTGTGA	18	GENIC	homozygous	53636109
8	61714443	61714444	A	G	32	GENIC	homozygous	53636110
8	61714488	61714489	C	T	23	GENIC	homozygous	53636111
8	61714949	61714950	C	-	14	GENIC	homozygous	53646620
8	61716019	61716020	G	T	20	GENIC	homozygous	53636112
8	61716135	61716136	C	T	13	GENIC	homozygous	53636113
8	61716313	61716314	G	GTTATTATTATTA	5	GENIC	homozygous	53646621
8	61716382	61716383	G	T	16	GENIC	homozygous	53636114
8	61715130	61715131	A	C	26	GENIC	homozygous	52988697
8	61716603	61716604	G	T	18	GENIC	homozygous	53636115
8	61716664	61716665	T	C	20	GENIC	possibly homozygous	53636116
8	61717304	61717305	T	C	24	GENIC	homozygous	53123489
8	61717466	61717467	C	G	17	GENIC	homozygous	53123490
8	61717689	61717690	G	A	18	GENIC	possibly homozygous	53636117
8	61717713	61717714	T	G	23	GENIC	homozygous	53636118
8	61717760	61717761	G	A	29	GENIC	homozygous	53636119
8	61717770	61717771	T	G	29	GENIC	homozygous	53636120
8	61717785	61717786	T	-	22	GENIC	homozygous	52988718