chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	44736137	44736138	C	T	48	GENIC	homozygous	149047608
8	44736239	44736240	T	C	46	GENIC	homozygous	149047609
8	44736879	44736880	A	G	33	GENIC	homozygous	149047610
8	44736947	44736948	G	A	30	GENIC	homozygous	149047611
8	44737029	44737030	A	G	42	GENIC	homozygous	149047612
8	44737210	44737211	G	A	53	GENIC	homozygous	149047613
8	44737499	44737500	T	G	40	GENIC	homozygous	149047614
8	44738018	44738019	A	C	11	GENIC	heterozygous	403236269
8	44738018	44738019	A		11	GENIC	heterozygous	403236270
8	44738018	44738019	A	G	11	GENIC	possibly homozygous	403236271
8	44738020	44738021	A		11	GENIC	heterozygous	403236272
8	44738020	44738021	A	C	11	GENIC	possibly homozygous	403236273
8	44739249	44739250	A	T	31	GENIC	homozygous	149047615
8	44739869	44739870	G	A	33	GENIC	possibly homozygous	149047616
8	44740216	44740217	C	T	31	GENIC	homozygous	149047617
8	44740645	44740646	T	G	32	GENIC	homozygous	149047618
8	44740858	44740859	A	G	42	GENIC	homozygous	149047619
8	44741224	44741225	C	G	43	GENIC	homozygous	149047620
8	44741225	44741226	C	T	43	GENIC	homozygous	149047621
8	44741816	44741817	C	T	27	GENIC	homozygous	149047622
8	44741855	44741856	G	T	33	GENIC	homozygous	144819200