chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	40904947	40904948	A	G	9	GENIC	homozygous	109699535
19	40905626	40905627	C	T	30	GENIC	homozygous	109961954
19	40906341	40906342	A	C	31	GENIC	homozygous	109961956
19	40908682	40908683	G	A	42	GENIC	homozygous	109961958
19	40909097	40909098	A	G	39	GENIC	homozygous	109699547
19	40909802	40909803	C	T	44	GENIC	homozygous	109961960
19	40909333	40909334	A	G	34	GENIC	homozygous	110022068
19	40910937	40910938	C	T	19	GENIC	possibly homozygous	109961962
19	40911204	40911205	T	C	25	GENIC	homozygous	109699561
19	40911324	40911325	T	C	30	GENIC	homozygous	109699563
19	40911346	40911347	G	A	32	GENIC	homozygous	109961964
19	40911387	40911388	G	C	29	GENIC	homozygous	109961966
19	40912897	40912898	A	G	27	GENIC	possibly homozygous	109699567
19	40915147	40915148	A	C	27	GENIC	heterozygous	119629856
19	40918181	40918182	T	C	52	GENIC	homozygous	109699585
19	40920475	40920476	C	A	23	GENIC	homozygous	109961968
19	40920865	40920866	A	G	35	GENIC	homozygous	109699593
19	40921746	40921747	C	T	37	GENIC	homozygous	109699597
19	40925623	40925624	T	C	13	GENIC	homozygous	119629857
19	40923920	40923921	A	C	19	GENIC	homozygous	110170963
19	40917156	40917157	T	C	36	GENIC	homozygous	110065656