chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37873554	37873555	T	C	21	GENIC	homozygous	109694552
19	37874801	37874802	C	T	44	GENIC	homozygous	110049507
19	37875174	37875175	C	T	22	GENIC	homozygous	109694554
19	37877649	37877650	A	G	39	GENIC	homozygous	109694556
19	37877858	37877859	C	T	23	GENIC	homozygous	109694558
19	37879648	37879649	T	A	31	GENIC	homozygous	109694560
19	37882145	37882146	A	T	40	GENIC	homozygous	109694562
19	37882563	37882564	C	A	30	GENIC	homozygous	109924889
19	37882752	37882753	G	A	26	GENIC	homozygous	109694564
19	37883514	37883515	G	A	37	GENIC	homozygous	109694566
19	37883594	37883595	T	G	26	GENIC	homozygous	109694568
19	37884207	37884208	C	T	26	GENIC	homozygous	109694570
19	37885973	37885974	T	C	57	GENIC	homozygous	109694572
19	37889813	37889814	G	T	31	GENIC	heterozygous	119629265
19	37882910	37882911	C	T	19	GENIC	possibly homozygous	110065538
19	37882917	37882918	T	C	20	GENIC	homozygous	119629261
19	37882918	37882919	G	C	20	GENIC	homozygous	119629262
19	37884797	37884798	A	G	35	GENIC	heterozygous	119629263
19	37888449	37888450	G	A	49	GENIC	possibly homozygous	119629264
19	37889827	37889828	G	A	31	GENIC	heterozygous	119629266
19	37889837	37889838	C	T	30	GENIC	heterozygous	119629267
19	37889866	37889867	T	C	27	GENIC	heterozygous	119629268
19	37890231	37890232	A	G	47	GENIC	homozygous	109694574
19	37890371	37890372	A	G	55	GENIC	homozygous	109694576
19	37892417	37892418	G	A	66	GENIC	homozygous	109694578
19	37895585	37895586	A	G	42	GENIC	possibly homozygous	109694580
19	37897270	37897271	T	C	39	GENIC	homozygous	109694582
19	37899540	37899541	T	C	48	GENIC	homozygous	109694584
19	37899934	37899935	C	T	57	GENIC	homozygous	109694586
19	37900029	37900030	C	T	62	GENIC	homozygous	109694588
19	37900453	37900454	C	T	52	GENIC	homozygous	109694590
19	37902753	37902754	A	C	12	GENIC	heterozygous	110080506
19	37903515	37903516	A	G	46	GENIC	homozygous	109694592