chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	34116563	34116564	T	G	33	GENIC	possibly homozygous	147193374
19	34118597	34118597		TGCCTCT	44	GENIC	homozygous	145068324
19	34122274	34122275	T	C	52	GENIC	possibly homozygous	147193375
19	34131031	34131032	C	T	22	GENIC	homozygous	155124202
19	34131031	34131032	C		22	GENIC	heterozygous	403450115
19	34131039	34131040	C		21	GENIC	homozygous	403450116
19	34131039	34131040	C	T	21	GENIC	heterozygous	403450117
19	34131353	34131354	C	T	4	GENIC	homozygous	147193376
19	34131355	34131356	C	T	6	GENIC	heterozygous	403751933
19	34141741	34141742	G	A	36	GENIC	homozygous	145077542
19	34157595	34157596	C	T	49	GENIC	homozygous	147193378
19	34161065	34161066	T	G	60	GENIC	homozygous	145077549
19	34131038	34131043	TCTCT		21	GENIC	homozygous	140387321
19	34131049	34131049		C	24	GENIC	homozygous	140387322
19	34131049	34131050	T	C	25	GENIC	homozygous	140447680
19	34131056	34131057	T	A	26	GENIC	homozygous	140447681
19	34131357	34131357		TATATATATATATATATAT	6	GENIC	heterozygous	147310827