Variant report

Variant	esv3419177
Chromosome Location	chr11:104905032-104915298
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr11:104905693-104906006	GM12878	blood:	n/a	n/a
2	BATF	chr11:104905695-104905944	GM12878	blood:	n/a	n/a
3	BHLHE40	chr11:104914225-104914244	GM12878	blood:	n/a	n/a
4	BRCA1	chr11:104913608-104913870	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:104914457-104916305	Hela-S3	cervix:	n/a	chr11:104915784-104915797
6	CEBPB	chr11:104905287-104906325	Hela-S3	cervix:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
7	CEBPB	chr11:104905228-104906180	IMR90	lung:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
8	CEBPB	chr11:104913715-104914022	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:104905749-104906194	HepG2	liver:	n/a	chr11:104905915-104905932 chr11:104905919-104905930
10	CHD2	chr11:104912156-104912184	HepG2	liver:	n/a	n/a
11	CTCF	chr11:104905277-104905441	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr11:104910741-104910756	GM20000	blood:	n/a	n/a
13	CUX1	chr11:104905825-104905994	GM12878	blood:	n/a	n/a
14	E2F4	chr11:104905789-104906025	MCF10A-Er-Src	breast:	n/a	n/a
15	EBF1	chr11:104908982-104909357	GM12878	blood:	n/a	n/a
16	EBF1	chr11:104905700-104906374	GM12878	blood:	n/a	n/a
17	EBF1	chr11:104908962-104909342	GM12878	blood:	n/a	n/a
18	EP300	chr11:104905472-104906162	Hela-S3	cervix:	n/a	chr11:104905633-104905647
19	EP300	chr11:104914850-104915159	Hela-S3	cervix:	n/a	n/a
20	FOS	chr11:104905746-104906083	MCF10A-Er-Src	breast:	n/a	n/a
21	FOS	chr11:104905741-104906083	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr11:104914949-104915170	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
23	FOS	chr11:104905726-104906093	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr11:104914860-104915222	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104914879-104914888 chr11:104915099-104915109
25	FOS	chr11:104905732-104906076	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr11:104914952-104915225	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
27	FOS	chr11:104914969-104915169	MCF10A-Er-Src	breast:	n/a	chr11:104915099-104915109 chr11:104915096-104915107 chr11:104915099-104915109
28	FOXA1	chr11:104911365-104911826	HepG2	liver:	n/a	n/a
29	FOXA2	chr11:104911512-104911699	HepG2	liver:	n/a	n/a
30	GTF2F1	chr11:104905601-104906124	Hela-S3	cervix:	n/a	n/a
31	HNF4A	chr11:104911512-104911807	HepG2	liver:	n/a	n/a
32	IRF4	chr11:104905632-104906040	GM12878	blood:	n/a	chr11:104905869-104905883
33	JUN	chr11:104914201-104914344	K562	blood:	n/a	n/a
34	MAFK	chr11:104911377-104911627	HepG2	liver:	n/a	chr11:104911504-104911515 chr11:104911504-104911515 chr11:104911499-104911514
35	MAX	chr11:104905682-104906147	Hela-S3	cervix:	n/a	n/a
36	MYC	chr11:104905731-104906147	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr11:104905716-104906176	MCF10A-Er-Src	breast:	n/a	n/a
38	POLR2A	chr11:104905671-104905990	Hela-S3	cervix:	n/a	n/a
39	POLR2A	chr11:104908793-104908983	Hela-S3	cervix:	n/a	n/a
40	POLR2A	chr11:104905674-104906021	Hela-S3	cervix:	n/a	n/a
41	POLR2A	chr11:104905374-104906718	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr11:104905651-104906028	GM12878	blood:	n/a	n/a
43	POLR2A	chr11:104904887-104905211	GM12878	blood:	n/a	n/a
44	POLR2A	chr11:104905605-104906063	GM12891	blood:	n/a	n/a
45	POLR2A	chr11:104905713-104906010	GM12891	blood:	n/a	n/a
46	POLR2A	chr11:104905540-104905620	Hela-S3	cervix:	n/a	n/a
47	POLR2A	chr11:104914870-104915025	Hela-S3	cervix:	n/a	n/a
48	POLR2A	chr11:104907651-104907673	HUVEC	blood vessel:	n/a	n/a
49	POLR2A	chr11:104905702-104906053	GM12892	blood:	n/a	n/a
50	POLR2A	chr11:104908077-104910884	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104907029-104907079	GM12878	blood:	n/a
2	chr11:104907029-104907079	GM12878	blood:	n/a
3	chr11:104906381-104906431	AG09309	skin:	n/a
4	chr11:104906381-104906431	Hela-S3	cervix:	n/a
5	chr11:104905834-104905884	AG04450	lung:	fetal
6	chr11:104905889-104905939	RPTEC	kidney:	n/a
7	chr11:104905889-104905939	HMEC	breast:	n/a
8	chr11:104912363-104912413	BE2_C	brain:	n/a
9	chr11:104905834-104905884	PrEC	prostate:	n/a
10	chr11:104907029-104907079	HPAEpiC	pulmonary alveolar:	n/a
11	chr11:104906381-104906431	NT2-D1	testis:	n/a
12	chr11:104905834-104905884	Caco-2	colon:	n/a
13	chr11:104905834-104905884	HMEC	breast:	n/a
14	chr11:104905889-104905939	SK-N-SH_RA	brain:	n/a
15	chr11:104905834-104905884	GM12892	blood:	n/a
16	chr11:104912363-104912413	T-47D	breast:	n/a
17	chr11:104912363-104912413	HMEC	breast:	n/a
18	chr11:104907029-104907079	NH-A	brain:	n/a
19	chr11:104906381-104906431	HRCEpiC	kidney:	n/a
20	chr11:104905834-104905884	Hela-S3	cervix:	n/a
21	chr11:104905834-104905884	ovcar-3	ovarian:	n/a
22	chr11:104907029-104907079	SK-N-MC	brain:	n/a
23	chr11:104906381-104906431	H1-hESC	embryonic stem cell:	embryo
24	chr11:104907029-104907079	MCF-7	breast:	n/a
25	chr11:104905834-104905884	IMR90	lung:	fetal
26	chr11:104907029-104907079	AG10803	skin:	n/a
27	chr11:104906381-104906431	NH-A	brain:	n/a
28	chr11:104912363-104912413	K562	blood:	n/a
29	chr11:104906381-104906431	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:104905889-104905939	T-47D	breast:	n/a
31	chr11:104905834-104905884	HRCEpiC	kidney:	n/a
32	chr11:104905889-104905939	Caco-2	colon:	n/a
33	chr11:104905834-104905884	SK-N-SH_RA	brain:	n/a
34	chr11:104905889-104905939	Hepatocyte	liver:	n/a
35	chr11:104905834-104905884	HL-60	blood:	n/a
36	chr11:104906381-104906431	Caco-2	colon:	n/a
37	chr11:104905889-104905939	Hela-S3	cervix:	n/a
38	chr11:104905834-104905884	AG09309	skin:	n/a
39	chr11:104905834-104905884	NB4	blood:	n/a
40	chr11:104912363-104912413	MCF10A-Er-Src	breast:	n/a
41	chr11:104905889-104905939	K562	blood:	n/a
42	chr11:104907029-104907079	HCF	heart:	n/a
43	chr11:104905834-104905884	PANC-1	pancreas:	n/a
44	chr11:104912363-104912413	IMR90	lung:	fetal
45	chr11:104906381-104906431	AG10803	skin:	n/a
46	chr11:104906381-104906431	ProgFib	skin:	n/a
47	chr11:104905889-104905939	HPAEpiC	pulmonary alveolar:	n/a
48	chr11:104912363-104912413	NHDF-neo	bronchial:	n/a
49	chr11:104912363-104912413	HCF	heart:	n/a
50	chr11:104905889-104905939	HEEpiC	esophagus:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CARD16-1	chr11:104904935-104905085	NONHSAT023950

Variant related genes	Relation type
CASP1	TF binding region
CASP1	CpG island

Extended variants
information (count: 476 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:476 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539595	chr11:104905047-104905048	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs143162890	chr11:104905053-104905054	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs150883720	chr11:104905069-104905070	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs62640913	chr11:104905076-104905077	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
5	rs201044584	chr11:104905093-104905094	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs61755275	chr11:104905100-104905101	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs1042743	chr11:104905165-104905166	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs561394708	chr11:104905166-104905167	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs3016805	chr11:104905174-104905175	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs111937100	chr11:104905203-104905204	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs2509650	chr11:104905208-104905209	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs369601363	chr11:104905218-104905219	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs372339419	chr11:104905226-104905227	Weak transcription Active TSS Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs377723132	chr11:104905228-104905229	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs371354897	chr11:104905238-104905239	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs368787287	chr11:104905242-104905243	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs530319285	chr11:104905244-104905245	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs3018350	chr11:104905265-104905266	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs546835017	chr11:104905276-104905277	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs566992842	chr11:104905290-104905291	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs532495103	chr11:104905291-104905292	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs113689109	chr11:104905312-104905313	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs536909	chr11:104905316-104905317	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs181402286	chr11:104905367-104905368	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs537816562	chr11:104905401-104905402	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs554468068	chr11:104905407-104905408	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs568220313	chr11:104905413-104905414	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs148632250	chr11:104905438-104905439	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs553677043	chr11:104905454-104905455	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs576919029	chr11:104905459-104905460	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs545894907	chr11:104905496-104905497	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs556259045	chr11:104905506-104905507	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs576127890	chr11:104905516-104905517	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs142099152	chr11:104905551-104905552	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs561635474	chr11:104905588-104905589	Weak transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs550793479	chr11:104905605-104905606	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs369967257	chr11:104905671-104905672	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs565425374	chr11:104905688-104905689	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs183895258	chr11:104905702-104905703	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs7925706	chr11:104905709-104905710	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs188332258	chr11:104905712-104905713	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs112582828	chr11:104905753-104905754	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs376222697	chr11:104905772-104905773	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs199725474	chr11:104905802-104905803	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs150005656	chr11:104905834-104905835	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs370647445	chr11:104905846-104905847	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs200219743	chr11:104905858-104905859	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs373997855	chr11:104905885-104905886	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs368205186	chr11:104905889-104905890	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
50	rs180804835	chr11:104905890-104905891	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	20729466	CNVD
Cancer	21637783	CNVD
Acute myeloid leukemia	16864856	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21484798	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	20837533	CNVD
Breast cancer	21264507	CNVD
Cervical cancer	21063398	CNVD
Glioblastoma multiforme	19960244	CNVD
Liposarcoma	21253554	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Neuroblastoma	17533364	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Esophageal squamous carcinoma	18350619	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Neuroblastoma	18923191	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
Breast cancer	16608533	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Basal cell lymphoma	17053054	CNVD
Hepatocellular carcinoma	16785998	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21958427	CNVD
Lung cancer	18438408	CNVD
Ewing''s sarcoma	17952124	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17603634	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Basal cell lymphoma	16790693	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21364760	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Mental retardation	19966786	CNVD
Non-small cell lung cancer	21829676	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Intracranial aneurysm	16715129	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Ovarian cancer	21720365	CNVD
Chronic lymphocytic leukemia	17805327	CNVD
Glioblastoma multiforme	22286061	CNVD
Breast cancer	16397240	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Neuroblastoma	17327916	CNVD
Melanoma	17363583	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Mantle cell lymphoma	19029149	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant melanoma	17260012	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Prostate cancer	16573809	CNVD
Obesity	19966786	CNVD
Prostate cancer	18632612	CNVD

Chromatin state (count:574 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104894200-104905600	Weak transcription	Esophagus	oesophagus
2	chr11:104897800-104905600	Weak transcription	Ovary	ovary
3	chr11:104899200-104905400	Weak transcription	Aorta	Aorta
4	chr11:104899400-104905400	Weak transcription	Fetal Brain Male	brain
5	chr11:104899400-104905600	Weak transcription	Fetal Muscle Trunk	muscle
6	chr11:104899600-104905200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
7	chr11:104899600-104909200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:104902000-104905400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr11:104902200-104906800	Weak transcription	Gastric	stomach
10	chr11:104903000-104906000	Active TSS	Primary monocytes fromperipheralblood	blood
11	chr11:104903000-104906000	Active TSS	Duodenum Smooth Muscle	Duodenum
12	chr11:104903200-104906200	Active TSS	Rectal Mucosa Donor 29	rectum
13	chr11:104903200-104906200	Flanking Active TSS	Dnd41	blood
14	chr11:104903200-104906400	Active TSS	Rectal Smooth Muscle	rectum
15	chr11:104903400-104905200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
16	chr11:104903400-104905200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr11:104903400-104906000	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr11:104903400-104906000	Active TSS	GM12878-XiMat	blood
19	chr11:104903400-104906200	Active TSS	Primary T cells fromperipheralblood	blood
20	chr11:104903400-104906400	Active TSS	Right Atrium	heart
21	chr11:104903600-104905200	Flanking Active TSS	Primary T cells from cord blood	blood
22	chr11:104903600-104906200	Active TSS	Brain Hippocampus Middle	brain
23	chr11:104903800-104905200	Enhancers	Stomach Mucosa	stomach
24	chr11:104904000-104905200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
25	chr11:104904000-104905200	Flanking Active TSS	NHEK	skin
26	chr11:104904000-104905800	Active TSS	Colonic Mucosa	Colon
27	chr11:104904000-104906000	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr11:104904000-104906200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr11:104904200-104905200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr11:104904200-104905400	Flanking Active TSS	Primary B cells from peripheral blood	blood
31	chr11:104904200-104905400	Flanking Active TSS	HMEC	breast
32	chr11:104904200-104906000	Active TSS	Brain Anterior Caudate	brain
33	chr11:104904200-104906000	Active TSS	Colon Smooth Muscle	Colon
34	chr11:104904200-104906200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr11:104904200-104906200	Active TSS	Brain Cingulate Gyrus	brain
36	chr11:104904200-104906200	Active TSS	Stomach Smooth Muscle	stomach
37	chr11:104904400-104905200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chr11:104904400-104905400	Active TSS	Fetal Lung	lung
39	chr11:104904400-104905400	Weak transcription	Right Ventricle	heart
40	chr11:104904400-104905600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr11:104904400-104905800	Active TSS	Rectal Mucosa Donor 31	rectum
42	chr11:104904400-104905800	Active TSS	Skeletal Muscle Female	skeletal muscle
43	chr11:104904400-104906000	Active TSS	Breast Myoepithelial Primary Cells	Breast
44	chr11:104904400-104906000	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
45	chr11:104904400-104906000	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr11:104904400-104906000	Active TSS	Duodenum Mucosa	Duodenum
47	chr11:104904400-104906000	Active TSS	Fetal Intestine Small	intestine
48	chr11:104904400-104906000	Active TSS	Lung	lung
49	chr11:104904400-104906200	Active TSS	Primary T killer memory cells from peripheral blood	blood
50	chr11:104904400-104906200	Active TSS	Fetal Muscle Leg	muscle

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