chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	6039164	6039165	C	A	12	GENIC	homozygous	109763608
19	6045424	6045425	A	T	32	GENIC	homozygous	109627388
19	6112064	6112065	G	A	26	GENIC	homozygous	109627393
19	6137172	6137173	A	G	18	GENIC	homozygous	109627395
19	6142783	6142784	G	A	32	GENIC	homozygous	109627403
19	6143332	6143333	C	A	40	GENIC	homozygous	109627405
19	6147979	6147980	T	A	33	GENIC	homozygous	109763850
19	6147991	6147992	C	A	31	GENIC	homozygous	109763852
19	6148041	6148042	G	A	35	GENIC	homozygous	109627409
19	6148044	6148045	G	A	33	GENIC	homozygous	109627411
19	6154024	6154025	G	A	24	GENIC	homozygous	109763856
19	6154025	6154026	A	G	24	GENIC	homozygous	109763858
19	6186114	6186115	T	C	32	GENIC	heterozygous	109627417
19	6186161	6186162	C	T	29	GENIC	heterozygous	109627419
19	6235838	6235839	C	A	22	GENIC	homozygous	109627425
19	6284264	6284265	T	G	30	GENIC	homozygous	109627427
19	6284265	6284266	G	A	30	GENIC	homozygous	109627429
19	6284303	6284304	C	A	23	GENIC	homozygous	109627431
19	6284409	6284410	T	A	39	GENIC	homozygous	109627433
19	6195532	6195533	G	A	13	GENIC	heterozygous	109799224
19	6277146	6277147	T	G	25	GENIC	heterozygous	109799226
19	6301195	6301196	A	C	16	GENIC	heterozygous	109799229
19	6354147	6354148	G	T	44	GENIC	homozygous	109627437
19	6388739	6388740	G	T	20	GENIC	heterozygous	109799231