Variant report

Variant	nsv517089
Chromosome Location	chr11:104915563-104930676
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	ARID3A	chr11:104917801-104918523	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104922178-104922768	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104927775-104928650	HepG2	liver:	n/a	n/a
4	ATF3	chr11:104917796-104918302	A549	lung:	n/a	n/a
5	BATF	chr11:104915949-104916196	GM12878	blood:	n/a	n/a
6	BCL3	chr11:104917836-104918309	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
7	BCL3	chr11:104917818-104918400	A549	lung:	n/a	chr11:104917968-104917977 chr11:104917969-104917978
8	BRCA1	chr11:104917502-104918375	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:104928443-104928828	HepG2	liver:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
10	CEBPB	chr11:104915430-104916328	IMR90	lung:	n/a	chr11:104915784-104915797
11	CEBPB	chr11:104917654-104918310	A549	lung:	n/a	n/a
12	CEBPB	chr11:104917907-104918351	HepG2	liver:	n/a	n/a
13	CEBPB	chr11:104917575-104918420	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr11:104914457-104916305	Hela-S3	cervix:	n/a	chr11:104915784-104915797
15	CEBPB	chr11:104916752-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
16	CEBPB	chr11:104916648-104916931	HepG2	liver:	n/a	chr11:104916858-104916869
17	CEBPB	chr11:104916680-104917050	HepG2	liver:	n/a	chr11:104916858-104916869
18	CEBPB	chr11:104917671-104918417	IMR90	lung:	n/a	n/a
19	CEBPB	chr11:104917718-104918298	A549	lung:	n/a	n/a
20	CEBPB	chr11:104928569-104928699	IMR90	lung:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
21	CEBPB	chr11:104928584-104928787	A549	lung:	n/a	chr11:104928655-104928666 chr11:104928654-104928665
22	CEBPB	chr11:104926001-104926181	IMR90	lung:	n/a	chr11:104926116-104926127 chr11:104926116-104926129 chr11:104926060-104926071
23	CEBPB	chr11:104917592-104918391	A549	lung:	n/a	n/a
24	CEBPB	chr11:104925947-104926232	HepG2	liver:	n/a	chr11:104926116-104926127 chr11:104926116-104926129 chr11:104926060-104926071
25	CEBPB	chr11:104916699-104917013	IMR90	lung:	n/a	chr11:104916858-104916869
26	CEBPB	chr11:104918828-104918953	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr11:104922911-104923232	HepG2	liver:	n/a	chr11:104923066-104923077
28	CEBPB	chr11:104916683-104917034	Hela-S3	cervix:	n/a	chr11:104916858-104916869
29	CEBPD	chr11:104916761-104916943	HepG2	liver:	n/a	n/a
30	CHD2	chr11:104917679-104918334	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr11:104917693-104917895	A549	lung:	n/a	chr11:104917785-104917798
32	CREB1	chr11:104917957-104918170	A549	lung:	n/a	n/a
33	CTCF	chr11:104917320-104917470	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr11:104917320-104917470	NHDF-neo	bronchial:	n/a	n/a
35	CTCF	chr11:104917460-104917610	AG10803	skin:	n/a	n/a
36	CTCF	chr11:104917440-104917590	AG09319	gingival:	n/a	n/a
37	E2F4	chr11:104915974-104916280	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr11:104916685-104916931	MCF10A-Er-Src	breast:	n/a	n/a
39	E2F4	chr11:104917863-104918359	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F6	chr11:104917815-104918243	A549	lung:	n/a	n/a
41	EBF1	chr11:104915907-104916477	GM12878	blood:	n/a	n/a
42	EP300	chr11:104915951-104916258	Hela-S3	cervix:	n/a	n/a
43	EP300	chr11:104917677-104918422	A549	lung:	n/a	chr11:104918143-104918153
44	EP300	chr11:104928126-104928681	HepG2	liver:	n/a	n/a
45	EP300	chr11:104917518-104918404	Hela-S3	cervix:	n/a	chr11:104918143-104918153 chr11:104917608-104917622 chr11:104917603-104917617
46	EP300	chr11:104917645-104918417	A549	lung:	n/a	chr11:104918143-104918153
47	EP300	chr11:104922186-104922770	HepG2	liver:	n/a	n/a
48	EP300	chr11:104922175-104922695	HepG2	liver:	n/a	n/a
49	EP300	chr11:104915934-104916072	GM12878	blood:	n/a	n/a
50	EP300	chr11:104917837-104918381	HepG2	liver:	n/a	chr11:104918143-104918153

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104915759-104915809	AG09309	skin:	n/a
2	chr11:104915759-104915809	BJ	skin:	n/a
3	chr11:104916075-104916125	NH-A	brain:	n/a
4	chr11:104916331-104916381	SAEC	small airway:	n/a
5	chr11:104916773-104916823	HCM	heart:	n/a
6	chr11:104916773-104916823	HepG2	liver:	n/a
7	chr11:104916773-104916823	NH-A	brain:	n/a
8	chr11:104916773-104916823	AG04449	skin:	fetal
9	chr11:104915759-104915809	NB4	blood:	n/a
10	chr11:104916075-104916125	T-47D	breast:	n/a
11	chr11:104916018-104916068	SK-N-MC	brain:	n/a
12	chr11:104916331-104916381	NH-A	brain:	n/a
13	chr11:104915759-104915809	HEEpiC	esophagus:	n/a
14	chr11:104916018-104916068	NB4	blood:	n/a
15	chr11:104916773-104916823	HUVEC	blood vessel:	n/a
16	chr11:104916018-104916068	K562	blood:	n/a
17	chr11:104916331-104916381	HCM	heart:	n/a
18	chr11:104916331-104916381	HEK293	kidney:	embryo
19	chr11:104915759-104915809	HRCEpiC	kidney:	n/a
20	chr11:104915759-104915809	HCPEpiC	choroid plexus:	n/a
21	chr11:104916773-104916823	HCPEpiC	choroid plexus:	n/a
22	chr11:104916018-104916068	Hepatocyte	liver:	n/a
23	chr11:104916018-104916068	NT2-D1	testis:	n/a
24	chr11:104915759-104915809	SKMC	muscle:	n/a
25	chr11:104916018-104916068	HRCEpiC	kidney:	n/a
26	chr11:104916331-104916381	HCF	heart:	n/a
27	chr11:104916018-104916068	AG04449	skin:	fetal
28	chr11:104916075-104916125	BE2_C	brain:	n/a
29	chr11:104916075-104916125	SAEC	small airway:	n/a
30	chr11:104916018-104916068	ECC-1	luminal epithelium:	n/a
31	chr11:104916075-104916125	HCT-116	colon:	n/a
32	chr11:104916075-104916125	SKMC	muscle:	n/a
33	chr11:104916773-104916823	RPTEC	kidney:	n/a
34	chr11:104916018-104916068	HCM	heart:	n/a
35	chr11:104916331-104916381	SK-N-MC	brain:	n/a
36	chr11:104916773-104916823	BJ	skin:	n/a
37	chr11:104916773-104916823	U87	brain:	n/a
38	chr11:104916075-104916125	NB4	blood:	n/a
39	chr11:104916018-104916068	HL-60	blood:	n/a
40	chr11:104916075-104916125	HepG2	liver:	n/a
41	chr11:104916773-104916823	HRPEpiC	eye:	n/a
42	chr11:104916018-104916068	BE2_C	brain:	n/a
43	chr11:104916018-104916068	NHDF-neo	bronchial:	n/a
44	chr11:104916018-104916068	BJ	skin:	n/a
45	chr11:104916773-104916823	AG09309	skin:	n/a
46	chr11:104916018-104916068	HIPEpiC	eye:	n/a
47	chr11:104915759-104915809	HRPEpiC	eye:	n/a
48	chr11:104916773-104916823	PANC-1	pancreas:	n/a
49	chr11:104916075-104916125	AG04450	lung:	fetal
50	chr11:104916018-104916068	AG04450	lung:	fetal

Variant related genes	Relation type
CARD16	TF binding region
CARD16	CpG island

Extended variants
information (count: 640 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:640 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10895763	chr11:104915563-104915564	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544760853	chr11:104915566-104915567	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs139184839	chr11:104915572-104915573	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs575244316	chr11:104915598-104915599	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs544222100	chr11:104915659-104915660	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs376957386	chr11:104915674-104915675	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs142384638	chr11:104915711-104915712	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs529678770	chr11:104915722-104915723	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs184863128	chr11:104915742-104915743	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs189241130	chr11:104915759-104915760	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs528706053	chr11:104915760-104915761	Weak transcription Active TSS Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs112479312	chr11:104915800-104915801	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs143469664	chr11:104915817-104915818	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs10598126	chr11:104915818-104915819	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs551996792	chr11:104915820-104915821	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs560532938	chr11:104915821-104915822	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs7933945	chr11:104915844-104915845	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs549235240	chr11:104915879-104915880	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs181595695	chr11:104915899-104915900	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs372547357	chr11:104915934-104915935	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs375786261	chr11:104915977-104915978	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs369131636	chr11:104915989-104915990	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs372915799	chr11:104915993-104915994	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs376119781	chr11:104915997-104915998	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs184787523	chr11:104916003-104916004	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs375363890	chr11:104916014-104916015	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs141990846	chr11:104916016-104916017	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs150516068	chr11:104916018-104916019	Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs200512282	chr11:104916041-104916042	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
30	rs200999612	chr11:104916043-104916044	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
31	rs371598262	chr11:104916057-104916058	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
32	rs189692884	chr11:104916060-104916061	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
33	rs201968553	chr11:104916074-104916075	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs180923379	chr11:104916075-104916076	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
35	rs543986535	chr11:104916139-104916140	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs139445248	chr11:104916175-104916176	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs574487312	chr11:104916184-104916185	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs540195143	chr11:104916189-104916190	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs560130275	chr11:104916205-104916206	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs537011943	chr11:104916223-104916224	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs573575145	chr11:104916238-104916239	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557039997	chr11:104916247-104916248	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs545613954	chr11:104916248-104916249	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs561513494	chr11:104916285-104916286	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs565322932	chr11:104916314-104916315	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs577266750	chr11:104916332-104916333	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
47	rs376393069	chr11:104916344-104916345	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs550820321	chr11:104916358-104916359	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs546122012	chr11:104916426-104916427	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs185971161	chr11:104916430-104916431	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	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:348 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104906600-104915600	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chr11:104910200-104915800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr11:104912200-104915600	Weak transcription	Placenta	Placenta
4	chr11:104912400-104915800	Weak transcription	HepG2	liver
5	chr11:104912600-104917800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
6	chr11:104912600-104920800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr11:104913000-104916200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
8	chr11:104913600-104915600	Flanking Active TSS	Dnd41	blood
9	chr11:104913600-104916200	Active TSS	Hela-S3	cervix
10	chr11:104913600-104916400	Flanking Active TSS	Primary mononuclear cells fromperipheralblood	Blood
11	chr11:104913600-104916600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chr11:104913800-104915600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
13	chr11:104913800-104916000	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr11:104913800-104916200	Active TSS	Primary T cells fromperipheralblood	blood
15	chr11:104914000-104916200	Active TSS	Rectal Mucosa Donor 29	rectum
16	chr11:104914000-104916600	Active TSS	Duodenum Smooth Muscle	Duodenum
17	chr11:104914200-104915600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr11:104914200-104915800	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
19	chr11:104914200-104916000	Active TSS	Lung	lung
20	chr11:104914200-104916000	Active TSS	Right Ventricle	heart
21	chr11:104914200-104916000	Active TSS	GM12878-XiMat	blood
22	chr11:104914200-104916200	Active TSS	Colonic Mucosa	Colon
23	chr11:104914200-104916400	Active TSS	Ovary	ovary
24	chr11:104914200-104916400	Flanking Active TSS	HUVEC	blood vessel
25	chr11:104914200-104916600	Active TSS	Rectal Smooth Muscle	rectum
26	chr11:104914400-104915600	Enhancers	NHEK	skin
27	chr11:104914400-104915800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
28	chr11:104914400-104916200	Active TSS	Primary T killer memory cells from peripheral blood	blood
29	chr11:104914400-104916400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
30	chr11:104914400-104916400	Active TSS	Brain Hippocampus Middle	brain
31	chr11:104914400-104916400	Active TSS	Fetal Muscle Leg	muscle
32	chr11:104914400-104916400	Active TSS	Stomach Smooth Muscle	stomach
33	chr11:104914600-104915600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr11:104914600-104915600	Weak transcription	Esophagus	oesophagus
35	chr11:104914600-104915600	Weak transcription	Fetal Intestine Large	intestine
36	chr11:104914600-104915600	Weak transcription	Fetal Stomach	stomach
37	chr11:104914600-104915600	Weak transcription	Fetal Thymus	thymus
38	chr11:104914600-104915600	Weak transcription	Skeletal Muscle Male	skeletal muscle
39	chr11:104914600-104916200	Active TSS	Primary monocytes fromperipheralblood	blood
40	chr11:104914600-104916200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
41	chr11:104914600-104916200	Active TSS	Primary T helper naive cells from peripheral blood	blood
42	chr11:104914600-104916200	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
43	chr11:104914600-104916200	Active TSS	Fetal Lung	lung
44	chr11:104914600-104916200	Active TSS	Left Ventricle	heart
45	chr11:104914600-104916200	Active TSS	Thymus	Thymus
46	chr11:104914600-104916200	Active TSS	Monocytes-CD14+_RO01746	blood
47	chr11:104914600-104916200	Active TSS	NHLF	lung
48	chr11:104914600-104916400	Active TSS	Right Atrium	heart
49	chr11:104914600-104916600	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:104914600-104918000	Weak transcription	Gastric	stomach

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