Variant report

Variant	nsv898032
Chromosome Location	chr11:84274481-84364527
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	chr11:84275511-84276096	HepG2	liver:	n/a	n/a
2	BCL3	chr11:84275350-84276036	A549	lung:	n/a	chr11:84275514-84275527
3	CEBPB	chr11:84348157-84348515	MCF-7	breast:	n/a	n/a
4	CEBPB	chr11:84362186-84362420	HepG2	liver:	n/a	chr11:84362314-84362325
5	CEBPB	chr11:84344635-84344903	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr11:84275681-84276045	MCF-7	breast:	n/a	chr11:84275854-84275866
7	CEBPB	chr11:84275253-84276015	A549	lung:	n/a	chr11:84275854-84275866
8	CEBPB	chr11:84323811-84324041	A549	lung:	n/a	n/a
9	CEBPB	chr11:84323767-84324051	IMR90	lung:	n/a	n/a
10	CHD1	chr11:84359471-84359655	H1-hESC	embryonic stem cell:	n/a	n/a
11	CHD2	chr11:84359510-84359789	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr11:84275666-84275949	A549	lung:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
13	CTCF	chr11:84275760-84275910	HRPEpiC	eye:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
14	CTCF	chr11:84275780-84275930	GM12864	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
15	CTCF	chr11:84275680-84275830	HFF	foreskin:	n/a	n/a
16	CTCF	chr11:84275740-84275890	GM12867	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
17	CTCF	chr11:84275706-84275968	H1-hESC	embryonic stem cell:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
18	CTCF	chr11:84275760-84275893	MCF-7	breast:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
19	CTCF	chr11:84275760-84275910	HCPEpiC	choroid plexus:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
20	CTCF	chr11:84275717-84275950	GM13976	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
21	CTCF	chr11:84275740-84275890	HA-sp	spinal cord:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
22	CTCF	chr11:84275696-84275921	HepG2	liver:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
23	CTCF	chr11:84276120-84276270	AG04450	lung:	n/a	n/a
24	CTCF	chr11:84275740-84275890	GM12865	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
25	CTCF	chr11:84275722-84275958	Lung_OC	lung:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
26	CTCF	chr11:84275300-84275450	HA-sp	spinal cord:	n/a	n/a
27	CTCF	chr11:84275760-84275910	GM12864	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
28	CTCF	chr11:84275740-84275890	A549	lung:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
29	CTCF	chr11:84275580-84276073	HCT-116	colon:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
30	CTCF	chr11:84310993-84311009	MCF-7	breast:	n/a	n/a
31	CTCF	chr11:84275740-84275890	GM12874	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
32	CTCF	chr11:84275624-84276056	GM12878	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
33	CTCF	chr11:84275720-84275870	HEK293	kidney:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
34	CTCF	chr11:84275742-84275929	Fibrobl	skin:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
35	CTCF	chr11:84275627-84275972	A549	lung:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
36	CTCF	chr11:84275715-84275947	ProgFib	skin:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
37	CTCF	chr11:84353600-84353750	HMEC	breast:	n/a	n/a
38	CTCF	chr11:84275683-84275995	T-47D	breast:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
39	CTCF	chr11:84275760-84275910	GM12875	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
40	CTCF	chr11:84275380-84275530	K562	blood:	n/a	n/a
41	CTCF	chr11:84275720-84275870	HepG2	liver:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
42	CTCF	chr11:84275800-84275950	K562	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
43	CTCF	chr11:84275660-84275810	HVMF	connective:	n/a	n/a
44	CTCF	chr11:84353559-84353987	MCF-7	breast:	n/a	n/a
45	CTCF	chr11:84275740-84275890	HUVEC	blood vessel:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
46	CTCF	chr11:84275300-84275450	GM12873	blood:	n/a	n/a
47	CTCF	chr11:84275740-84275890	HRE	kidney:	n/a	chr11:84275823-84275841 chr11:84275818-84275839 chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840
48	CTCF	chr11:84275711-84275973	GM13977	blood:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
49	CTCF	chr11:84275780-84275930	AG04450	lung:	n/a	chr11:84275826-84275836 chr11:84275825-84275838 chr11:84275824-84275840 chr11:84275818-84275839 chr11:84275823-84275841
50	CTCF	chr11:84353660-84353814	Pancreas_OC	pancreas:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:93644235..93646681-chr11:84291814..84294757,2	MCF-7	breast:
2	chr11:84276005..84278471-chr11:84278916..84281789,2	MCF-7	breast:
3	chr11:84280312..84283130-chr11:84397090..84398747,2	MCF-7	breast:
4	chr11:84270260..84272879-chr11:84274158..84275697,2	MCF-7	breast:
5	chr11:84353205..84353720-chr11:84425398..84425994,2	MCF-7	breast:
6	chr11:84189421..84191994-chr11:84344935..84346949,2	K562	blood:
7	chr11:84275372..84277697-chr11:84285469..84287764,2	MCF-7	breast:
8	chr11:84274871..84276645-chr11:84399735..84401764,2	MCF-7	breast:
9	chr11:84331138..84333435-chr11:84335070..84336860,2	MCF-7	breast:
10	chr11:84341502..84343647-chr11:84513297..84515436,2	MCF-7	breast:
11	chr11:84360777..84362282-chr11:84396654..84399433,2	MCF-7	breast:
12	chr11:84300252..84301852-chr20:44562051..44563883,2	MCF-7	breast:
13	chr11:84276005..84278471-chr11:84278916..84281789,2	MCF-7	breast:
14	chr11:84310262..84312243-chr11:84312847..84315760,2	MCF-7	breast:
15	chr11:84266119..84270134-chr11:84272425..84277265,4	MCF-7	breast:
16	chr11:84275372..84277697-chr11:84285469..84287764,2	MCF-7	breast:
17	chr11:84353266..84354226-chr11:84425005..84426301,12	MCF-7	breast:
18	chr11:84346226..84348368-chr11:84348701..84351373,2	MCF-7	breast:
19	chr11:84265904..84268550-chr11:84272866..84275425,2	K562	blood:
20	chr11:84101555..84102182-chr11:84275381..84276078,3	MCF-7	breast:
21	chr11:84260699..84261603-chr11:84275042..84275969,2	MCF-7	breast:
22	chr11:84331138..84333435-chr11:84335070..84336860,2	MCF-7	breast:
23	chr11:84310262..84312243-chr11:84312847..84315760,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000240174	TF binding region
ENSG00000100982	chromatin interactions
ENSG00000117500	chromatin interactions
ENSG00000122483	chromatin interactions
ENSG00000240174	chromatin interactions

Extended variants
information (count: 3164 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:3164 , 50 per page) page: 1 2 3 4 5 6 7 ... 64

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs948141	chr11:84274481-84274482	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374516088	chr11:84274521-84274522	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs555632549	chr11:84274562-84274563	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs191903965	chr11:84274586-84274587	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529043919	chr11:84274621-84274622	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79519706	chr11:84274636-84274637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs79697430	chr11:84274665-84274666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539718616	chr11:84274673-84274674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs557671762	chr11:84274704-84274705	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs566118260	chr11:84274710-84274711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs533572027	chr11:84274730-84274731	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs532299195	chr11:84274741-84274742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs573698658	chr11:84274871-84274872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs76728208	chr11:84274902-84274903	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs562530299	chr11:84274912-84274913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147187096	chr11:84274953-84274954	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183761006	chr11:84275003-84275004	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs188292361	chr11:84275008-84275009	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs61898962	chr11:84275023-84275024	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs540646965	chr11:84275079-84275080	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs561999779	chr11:84275111-84275112	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs529392803	chr11:84275167-84275168	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs532023050	chr11:84275185-84275186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs61898963	chr11:84275198-84275199	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs562694492	chr11:84275210-84275211	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs140029136	chr11:84275221-84275222	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs149590927	chr11:84275233-84275234	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs566453572	chr11:84275238-84275239	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs181939327	chr11:84275253-84275254	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs187570828	chr11:84275254-84275255	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12421357	chr11:84275262-84275263	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs190506348	chr11:84275334-84275335	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181782381	chr11:84275345-84275346	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs34410709	chr11:84275401-84275402	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs575769460	chr11:84275414-84275415	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs540059035	chr11:84275427-84275428	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs148722683	chr11:84275444-84275445	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs533730336	chr11:84275467-84275468	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs573588198	chr11:84275482-84275483	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs11827703	chr11:84275493-84275494	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs562111135	chr11:84275523-84275524	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs186034199	chr11:84275527-84275528	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs544678823	chr11:84275578-84275579	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs573867955	chr11:84275580-84275581	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs532935225	chr11:84275596-84275597	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs551180838	chr11:84275633-84275634	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs534966675	chr11:84275637-84275638	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs190095657	chr11:84275663-84275664	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs549045542	chr11:84275743-84275744	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs547406875	chr11:84275768-84275769	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	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
Multiple myeloma	16461302	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Cervical cancer	21062161	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	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
Multiple myeloma	16616336	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	22429812	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Ovarian neoplasms	16753589	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	20844748	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Colorectal cancer	16912164	CNVD
Mental retardation	17847001	CNVD
Melanoma	19509136	CNVD
Sudden cardiac death	19188705	CNVD
Prostate cancer	16573809	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
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Cancer	20164920	CNVD
Obesity	20622171	CNVD
Breast cancer	22522925	CNVD
Developmental delay	21147756	CNVD
Bipolar disorder	19114987	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Ductal carcinoma	22052326	CNVD
Autism	19246517	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Breast cancer	17142309	CNVD

Chromatin state (count:282 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:84264400-84280600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chr11:84269800-84275000	Weak transcription	Fetal Intestine Small	intestine
3	chr11:84270000-84275000	Weak transcription	Fetal Intestine Large	intestine
4	chr11:84270200-84275000	Weak transcription	HepG2	liver
5	chr11:84271600-84275000	Weak transcription	Fetal Brain Male	brain
6	chr11:84271800-84277800	Weak transcription	Brain Germinal Matrix	brain
7	chr11:84273600-84274600	Weak transcription	Liver	Liver
8	chr11:84273800-84274600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr11:84274200-84275600	Enhancers	Fetal Brain Female	brain
10	chr11:84274200-84275800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr11:84274400-84274800	Enhancers	Brain Angular Gyrus	brain
12	chr11:84274400-84274800	Enhancers	Stomach Smooth Muscle	stomach
13	chr11:84274400-84275000	Enhancers	A549	lung
14	chr11:84274400-84275200	Enhancers	Pancreatic Islets	Pancreatic Islet
15	chr11:84274400-84275400	Enhancers	Brain Hippocampus Middle	brain
16	chr11:84274400-84275800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr11:84274600-84275200	Enhancers	Brain Cingulate Gyrus	brain
18	chr11:84274600-84275200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
19	chr11:84274600-84275400	Enhancers	Brain Anterior Caudate	brain
20	chr11:84274600-84275600	Enhancers	Liver	Liver
21	chr11:84274800-84275200	Weak transcription	Stomach Smooth Muscle	stomach
22	chr11:84275000-84275400	Enhancers	Fetal Brain Male	brain
23	chr11:84275000-84275600	Enhancers	Fetal Intestine Large	intestine
24	chr11:84275000-84275600	Enhancers	Fetal Intestine Small	intestine
25	chr11:84275000-84275600	Enhancers	HepG2	liver
26	chr11:84275000-84275800	Flanking Active TSS	A549	lung
27	chr11:84275200-84275600	Enhancers	Stomach Smooth Muscle	stomach
28	chr11:84275200-84275800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr11:84275200-84275800	Enhancers	Duodenum Smooth Muscle	Duodenum
30	chr11:84275200-84275800	Active TSS	Pancreatic Islets	Pancreatic Islet
31	chr11:84275200-84276000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr11:84275400-84275800	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr11:84275600-84275800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
34	chr11:84275800-84277000	Enhancers	A549	lung
35	chr11:84275800-84277400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr11:84275800-84277400	Weak transcription	Pancreatic Islets	Pancreatic Islet
37	chr11:84275800-84277600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr11:84275800-84277600	Weak transcription	Cortex derived primary cultured neurospheres	brain
39	chr11:84276000-84277400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr11:84276000-84277600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chr11:84276800-84277600	Enhancers	Primary hematopoietic stem cells short term culture	blood
42	chr11:84277000-84277400	Weak transcription	A549	lung
43	chr11:84277000-84278600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chr11:84277200-84278400	Enhancers	Primary hematopoietic stem cells	blood
45	chr11:84277400-84277800	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr11:84277400-84277800	Enhancers	A549	lung
47	chr11:84277400-84278600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr11:84277400-84278600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr11:84277400-84278800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
50	chr11:84277600-84278000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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