chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
19	37129080	37129081	A	G	34	GENIC	homozygous	109693028
19	37129331	37129332	G	A	15	GENIC	homozygous	109693030
19	37129570	37129571	C	G	17	GENIC	possibly homozygous	109693032
19	37129872	37129873	T	A	25	GENIC	possibly homozygous	109693034
19	37130134	37130135	A	G	22	GENIC	possibly homozygous	109693036
19	37130550	37130551	A	T	11	GENIC	heterozygous	110145786
19	37131402	37131403	A	C	24	GENIC	possibly homozygous	109693038
19	37133922	37133923	T	A	22	GENIC	homozygous	109693040
19	37133956	37133957	A	G	24	GENIC	homozygous	109693042
19	37134247	37134248	A	T	20	GENIC	homozygous	109693044
19	37138579	37138580	T	G	17	GENIC	possibly homozygous	109693046
19	37141019	37141020	A	G	15	GENIC	possibly homozygous	109693048
19	37141220	37141221	A	T	32	GENIC	homozygous	109693050
19	37141238	37141239	C	G	32	GENIC	possibly homozygous	109693052
19	37148202	37148203	A	G	25	GENIC	heterozygous	109693060
19	37145147	37145148	C	T	23	GENIC	possibly homozygous	109693054
19	37145713	37145714	T	G	23	GENIC	possibly homozygous	109693056
19	37146815	37146816	G	A	6	GENIC	homozygous	109693058
19	37150024	37150025	A	G	22	GENIC	possibly homozygous	109693062
19	37153586	37153587	A	G	31	GENIC	possibly homozygous	109693066
19	37160824	37160825	A	G	24	GENIC	homozygous	109693070
19	37162115	37162116	C	G	25	GENIC	possibly homozygous	109693072
19	37163282	37163283	G	A	19	GENIC	homozygous	109693074
19	37165609	37165610	A	G	27	GENIC	possibly homozygous	109693076
19	37168875	37168876	G	A	28	GENIC	homozygous	109693078
19	37170491	37170492	G	A	35	GENIC	possibly homozygous	109693080
19	37170912	37170913	G	A	22	GENIC	homozygous	109693082
19	37158208	37158209	A	G	25	GENIC	possibly homozygous	109924574
19	37163244	37163245	C	T	29	GENIC	homozygous	109961665