chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	76918809	76918810	C	A	57	GENIC	homozygous	138345903
8	76919072	76919073	G	A	50	GENIC	homozygous	144823753
8	76920655	76920656	T	C	41	GENIC	homozygous	138345904
8	76920719	76920720	C	A	37	GENIC	homozygous	144823754
8	76920923	76920924	G	A	40	GENIC	homozygous	144823755
8	76921111	76921112	C	G	46	GENIC	homozygous	138345905
8	76921371	76921371		T	46	GENIC	homozygous	138249065
8	76921940	76921941	C	T	46	GENIC	possibly homozygous	144823756
8	76923283	76923284	G	A	51	GENIC	homozygous	138345906
8	76923689	76923690	C	A	51	GENIC	homozygous	138345907
8	76924072	76924073	G	A	50	GENIC	homozygous	138345908
8	76924263	76924264	C	T	58	GENIC	homozygous	144823757
8	76924845	76924846	G	T	43	GENIC	homozygous	144823758
8	76924986	76924987	G	A	42	GENIC	homozygous	138345909
8	76925128	76925129	T	C	39	GENIC	possibly homozygous	138345910
8	76925195	76925196	G	A	35	GENIC	homozygous	138345911
8	76925201	76925202	C	T	35	GENIC	homozygous	138345912
8	76925214	76925215	G	A	33	GENIC	homozygous	138345913
8	76925235	76925236	G	A	34	GENIC	homozygous	138345914
8	76925333	76925334	G	A	33	GENIC	homozygous	138345915
8	76925338	76925339	G	A	35	GENIC	homozygous	138345916
8	76925671	76925672	T	G	35	GENIC	homozygous	138345917
8	76925683	76925684	G	A	37	GENIC	homozygous	138345918
8	76926545	76926546	C	T	50	GENIC	homozygous	138345919
8	76926563	76926563		AATCAACCAACC	51	GENIC	homozygous	138249066
8	76925516	76925519	ATA		24	GENIC	possibly homozygous	144812879
8	76935285	76935286	C		30	GENIC	heterozygous	403241409
8	76935285	76935286	C	T	30	GENIC	possibly homozygous	154515697
8	76923487	76923488	A	G	35	GENIC	heterozygous	154515695
8	76923487	76923488	A		35	GENIC	homozygous	403241406
8	76960295	76960296	A	G	25	GENIC	homozygous	144823759