chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	44760855	44760856	G	A	56	GENIC	homozygous	147405477
8	44761813	44761814	G	A	51	GENIC	homozygous	147405478
8	44761833	44761834	C	T	46	GENIC	homozygous	147405479
8	44762019	44762020	T	A	20	GENIC	homozygous	147405480
8	44762020	44762021	A	C	20	GENIC	homozygous	147405481
8	44763193	44763194	T	C	49	GENIC	homozygous	147405482
8	44764081	44764082	A	G	34	GENIC	homozygous	147405483
8	44765205	44765206	A	G	35	GENIC	homozygous	144819213
8	44765635	44765636	T	A	30	GENIC	homozygous	144819214
8	44766066	44766067	T	C	36	GENIC	homozygous	147405484
8	44766700	44766701	T	C	41	GENIC	possibly homozygous	147405485
8	44766769	44766770	G	A	45	GENIC	homozygous	147405486
8	44767176	44767177	C	G	17	GENIC	heterozygous	147405487
8	44767178	44767179	C	G	22	GENIC	heterozygous	144819215
8	44767925	44767926	G	A	44	GENIC	homozygous	147405488
8	44767172	44767173	C		17	GENIC	heterozygous	403236281
8	44767172	44767173	C	G	17	GENIC	heterozygous	403236282
8	44765614	44765629	ATATATATATATATA		26	GENIC	homozygous	147404474
8	44766557	44766568	AACCAACCAAC		35	GENIC	homozygous	147404475