chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	29899947	29899948	A	G	32	GENIC	homozygous	109160943
20	29902835	29902836	A	T	37	GENIC	homozygous	109160945
20	29904025	29904026	C	T	44	GENIC	homozygous	109251525
20	29906646	29906647	C	T	34	GENIC	homozygous	109160949
20	29908265	29908266	G	A	27	GENIC	homozygous	109251527
20	29909194	29909195	T	G	24	GENIC	possibly homozygous	109160951
20	29909583	29909584	C	T	35	GENIC	homozygous	109251529
20	29909584	29909585	C	T	34	GENIC	homozygous	109251531
20	29909830	29909831	G	A	33	GENIC	homozygous	109251533
20	29910036	29910037	A	G	31	GENIC	homozygous	109160953
20	29910418	29910419	C	T	23	GENIC	homozygous	109251535
20	29912671	29912672	A	T	38	GENIC	homozygous	109251537
20	29912724	29912725	T	C	42	GENIC	homozygous	109251539
20	29912784	29912785	A	T	43	GENIC	homozygous	109160959
20	29913482	29913483	G	C	39	GENIC	homozygous	109160963
20	29913701	29913702	C	T	36	GENIC	homozygous	109251541
20	29915039	29915040	G	A	19	GENIC	homozygous	109251543
20	29916871	29916872	T	C	41	GENIC	homozygous	109251547
20	29917449	29917450	T	C	11	GENIC	homozygous	109160965
20	29919406	29919407	T	A	23	GENIC	homozygous	109160967
20	29919821	29919822	A	G	36	GENIC	homozygous	109160969
20	29920499	29920500	T	C	34	GENIC	homozygous	109160971
20	29921040	29921041	T	C	34	GENIC	homozygous	109251549
20	29921488	29921489	C	T	29	GENIC	homozygous	109251551
20	29921636	29921637	T	C	44	GENIC	homozygous	109160975
20	29921637	29921638	G	C	44	GENIC	homozygous	109251553
20	29922628	29922629	G	T	31	GENIC	homozygous	109251555