chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37307028	37307029	T	G	12	GENIC	homozygous	109693400
19	37307496	37307497	G	A	10	GENIC	homozygous	109693402
19	37307904	37307905	T	G	14	GENIC	homozygous	109693404
19	37309698	37309699	T	C	42	GENIC	homozygous	109693406
19	37310010	37310011	A	G	16	GENIC	homozygous	109693408
19	37310255	37310256	A	G	28	GENIC	homozygous	109693410
19	37310327	37310328	G	A	21	GENIC	homozygous	109693412
19	37310688	37310689	C	T	26	GENIC	homozygous	109693414
19	37313125	37313126	A	G	38	GENIC	homozygous	109693416
19	37316471	37316472	T	C	18	GENIC	homozygous	109693418
19	37317962	37317963	G	A	23	GENIC	homozygous	109693422
19	37318329	37318330	A	G	13	GENIC	homozygous	109693424
19	37318487	37318488	T	A	17	GENIC	homozygous	109693426
19	37319923	37319924	C	T	21	GENIC	homozygous	109693428
19	37319996	37319997	A	C	21	GENIC	homozygous	109693430
19	37320735	37320736	A	G	21	GENIC	homozygous	109693432
19	37321007	37321008	T	C	28	GENIC	homozygous	109693434
19	37321313	37321314	A	G	17	GENIC	homozygous	109693436
19	37321341	37321342	T	A	17	GENIC	homozygous	109693438
19	37321443	37321444	C	T	14	GENIC	homozygous	109693440
19	37321507	37321508	A	C	15	GENIC	homozygous	109693442
19	37321531	37321532	A	C	18	GENIC	homozygous	109693444
19	37321564	37321565	G	A	14	GENIC	homozygous	109693446
19	37322272	37322273	A	G	21	GENIC	homozygous	109693448
19	37322418	37322419	A	C	13	GENIC	homozygous	109693450
19	37323686	37323687	C	G	27	GENIC	homozygous	109693452
19	37324478	37324479	T	G	16	GENIC	homozygous	109924617