chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
18	15779681	15779682	A		20	GENIC	possibly homozygous	140211571
18	15779698	15779699	A	G	22	GENIC	homozygous	140271427
18	15779859	15779860	G	C	27	GENIC	homozygous	140271428
18	15780092	15780093	T	G	27	GENIC	homozygous	140271430
18	15780642	15780643	T	C	22	GENIC	homozygous	140271431
18	15781175	15781176	A	G	19	GENIC	homozygous	140271432
18	15781859	15781860	A	G	23	GENIC	homozygous	140271434
18	15782610	15782611	T	A	19	GENIC	homozygous	140271436
18	15782619	15782620	A	T	19	GENIC	homozygous	140271437
18	15783796	15783797	C	T	17	GENIC	homozygous	140271439
18	15784717	15784718	G	A	28	GENIC	homozygous	140271440
18	15784766	15784767	A	T	27	GENIC	homozygous	140271441
18	15785612	15785613	G	A	21	GENIC	possibly homozygous	140271442
18	15785934	15785935	G	A	28	GENIC	homozygous	140271443
18	15786225	15786226	C	T	26	GENIC	homozygous	140271445
18	15786543	15786544	A	G	25	GENIC	homozygous	140271446
18	15781115	15781115		GGGAAGGA	18	GENIC	homozygous	142628144
18	15785917	15785917		C	26	GENIC	possibly homozygous	144489243
18	15783796	15783797	C		17	GENIC	heterozygous	403430196
18	15782299	15782301	CC		8	GENIC	homozygous	144489242