chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	39131517	39131518	C	CCTCTCTCTCTCTCTCTCT	5	GENIC	homozygous	51180829
11	39132796	39132804	CTCACACG	--------	7	GENIC	homozygous	51180830
11	39134800	39134801	A	AG	3	GENIC	homozygous	50878172
11	39134939	39134940	G	A	11	GENIC	homozygous	50740952
11	39135070	39135071	G	C	17	GENIC	homozygous	50740953
11	39136006	39136010	GGAT	----	11	GENIC	homozygous	51180831
11	39136324	39136325	G	A	33	GENIC	homozygous	50740955
11	39136821	39136822	C	T	34	GENIC	homozygous	50740956
11	39138691	39138692	A	ATATTTTACACTTAT	34	GENIC	homozygous	50740957
11	39139725	39139726	A	G	19	GENIC	homozygous	50740958
11	39141676	39141677	A	AG	24	GENIC	homozygous	50740959
11	39142366	39142367	C	CA	16	GENIC	homozygous	50740960
11	39149261	39149262	A	AG	12	GENIC	homozygous	50740961
11	39150831	39150832	T	A	25	GENIC	homozygous	50740962
11	39151471	39151472	T	C	29	GENIC	homozygous	50740963
11	39152197	39152198	A	AGT	32	GENIC	homozygous	50740964
11	39152290	39152291	A	AGT	18	GENIC	homozygous	50740965
11	39154122	39154123	G	GTATATATA	2	GENIC	homozygous	51275953
11	39156617	39156618	C	T	28	GENIC	homozygous	50740966
11	39156826	39156828	GT	--	11	GENIC	heterozygous	51180832
11	39161401	39161402	T	C	25	GENIC	homozygous	50740968
11	39168428	39168429	T	TCA	14	GENIC	possibly homozygous	50740969
11	39171115	39171116	G	A	26	GENIC	homozygous	50740970
11	39171270	39171271	T	C	31	GENIC	homozygous	50740971
11	39171768	39171769	T	-	33	GENIC	homozygous	50740972
11	39172648	39172649	A	G	32	GENIC	homozygous	50740973
11	39173001	39173007	ACACAC	------	21	GENIC	heterozygous	51180833
11	39173003	39173007	ACAC	----	21	GENIC	heterozygous	51180834
11	39173401	39173402	G	A	38	GENIC	homozygous	50740975
11	39174162	39174163	T	G	36	GENIC	homozygous	50740976
11	39174200	39174202	AA	--	16	GENIC	homozygous	51003905
11	39174300	39174301	C	CT	34	GENIC	homozygous	50740978
11	39174303	39174304	A	T	35	GENIC	homozygous	50740979
11	39174509	39174510	G	A	39	GENIC	homozygous	50740980