chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	917204	917205	A	G	22	GENIC	homozygous	109623469
19	917498	917500	CC		42	GENIC	homozygous	129578511
19	918187	918188	T	C	45	GENIC	homozygous	109623471
19	918234	918235	A	G	42	GENIC	homozygous	109623473
19	918373	918374	G	A	23	GENIC	homozygous	109623475
19	918795	918796	C		46	GENIC	homozygous	129578512
19	919701	919702	G		28	GENIC	possibly homozygous	129578513
19	920310	920311	G	T	44	GENIC	homozygous	109623477
19	921381	921382	T	C	40	GENIC	homozygous	109623479
19	921568	921569	C	T	32	GENIC	homozygous	109623481
19	922120	922121	C	T	34	GENIC	homozygous	109623483
19	924166	924167	A	G	39	GENIC	homozygous	109623485
19	925435	925436	A	T	43	GENIC	homozygous	109623487
19	925525	925527	CT		48	GENIC	homozygous	129578514
19	926389	926390	C	G	47	GENIC	homozygous	109623489
19	930372	930373	A	G	54	GENIC	homozygous	109623491
19	930960	930961	G	A	40	GENIC	homozygous	109623493
19	931381	931382	T	C	29	GENIC	homozygous	109623495
19	931512	931513	G	A	38	GENIC	homozygous	109623497
19	932531	932532	C	T	46	GENIC	homozygous	109623499
19	933488	933489	T	C	58	GENIC	homozygous	109623501
19	933748	933749	A	G	48	GENIC	homozygous	109623503
19	933976	933977	G	A	35	GENIC	homozygous	109623505
19	936334	936335	G	A	41	GENIC	homozygous	109623507
19	937351	937352	A	T	46	GENIC	possibly homozygous	109623509
19	937442	937443	T	C	36	GENIC	possibly homozygous	109623511
19	938960	938961	C	G	41	GENIC	homozygous	109623513
19	936027	936028	C	T	53	GENIC	homozygous	109833113