chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	6045424	6045425	A	T	21	GENIC	homozygous	109627388
19	6112064	6112065	G	A	22	GENIC	homozygous	109627393
19	6137172	6137173	A	G	10	GENIC	homozygous	109627395
19	6140893	6140894	A	T	7	GENIC	homozygous	109627397
19	6142626	6142627	C	A	20	GENIC	homozygous	109763844
19	6143332	6143333	C	A	31	GENIC	homozygous	109627405
19	6147956	6147957	A	T	12	GENIC	homozygous	109763848
19	6147979	6147980	T	A	13	GENIC	homozygous	109763850
19	6147991	6147992	C	A	13	GENIC	homozygous	109763852
19	6148041	6148042	G	A	14	GENIC	homozygous	109627409
19	6148044	6148045	G	A	14	GENIC	homozygous	109627411
19	6154024	6154025	G	A	24	GENIC	homozygous	109763856
19	6154025	6154026	A	G	24	GENIC	homozygous	109763858
19	6235800	6235801	G	C	16	GENIC	homozygous	109840777
19	6235838	6235839	C	A	25	GENIC	homozygous	109627425
19	6242821	6242822	G	C	2	GENIC	homozygous	109974964
19	6242818	6242819	C	G	2	GENIC	homozygous	109956467
19	6284264	6284265	T	G	28	GENIC	homozygous	109627427
19	6284265	6284266	G	A	28	GENIC	homozygous	109627429
19	6284303	6284304	C	A	22	GENIC	homozygous	109627431
19	6284409	6284410	T	A	21	GENIC	homozygous	109627433
19	6354147	6354148	G	T	18	GENIC	homozygous	109627437