chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	130973999	130974000	T	A	12	GENIC	homozygous	116726588
8	130974379	130974380	A	G	11	GENIC	homozygous	116726589
8	130977666	130977667	A	G	8	GENIC	homozygous	116726590
8	130978613	130978614	C	T	4	GENIC	homozygous	116726591
8	130978916	130978917	G	A	5	GENIC	homozygous	116726592
8	130979116	130979117	A	G	8	GENIC	homozygous	116726593
8	130979267	130979268	G	A	6	GENIC	homozygous	116726594
8	130979753	130979754	G	A	8	GENIC	homozygous	116726595
8	130980000	130980001	A	G	5	GENIC	homozygous	116726596
8	130982603	130982604	A	G	8	GENIC	homozygous	116726599
8	130983239	130983240	G	A	8	GENIC	homozygous	116726600
8	130983529	130983530	T	C	19	GENIC	homozygous	116726601
8	130983537	130983538	A	G	14	GENIC	homozygous	116726602
8	130983987	130983988	T	A	14	GENIC	homozygous	116726603
8	130984051	130984052	A	T	15	GENIC	homozygous	116726604
8	130984054	130984055	T	C	14	GENIC	homozygous	116902399
8	130984346	130984347	G	A	8	GENIC	homozygous	116902401
8	130984348	130984349	A	G	8	GENIC	homozygous	117176347
8	130984510	130984511	G	A	6	GENIC	homozygous	116726605
8	130984792	130984793	C	T	16	GENIC	homozygous	116726606
8	130985007	130985008	G	A	12	GENIC	homozygous	116726607
8	130985507	130985508	A	T	17	GENIC	homozygous	116726608
8	130985958	130985959	G	A	13	GENIC	homozygous	116726609
8	130985960	130985961	T	C	13	GENIC	homozygous	116726610
8	130987189	130987190	C	T	15	GENIC	homozygous	117073759
8	130987198	130987199	T	A	12	GENIC	homozygous	117073760
8	130987248	130987249	C	T	10	GENIC	homozygous	116726611
8	130988601	130988602	C	T	10	GENIC	homozygous	116726612
8	130990451	130990452	A	G	11	GENIC	homozygous	116726613
8	130990751	130990752	A	T	12	GENIC	homozygous	116726614
8	130991135	130991136	A	G	11	GENIC	homozygous	116726615
8	130992642	130992643	T	C	7	GENIC	homozygous	116726616
8	130999086	130999087	G	T	8	GENIC	homozygous	116726617
8	131000089	131000090	A	G	11	GENIC	homozygous	116726618
8	130989247	130989248	T	A	10	GENIC	homozygous	117913213