Variant report

Variant	esv1825856
Chromosome Location	chr11:105672706-105775768
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	CEBPB	chr11:105728547-105728818	IMR90	lung:	n/a	chr11:105728705-105728716
2	CEBPB	chr11:105738577-105738783	HepG2	liver:	n/a	n/a
3	CEBPB	chr11:105728616-105728816	HepG2	liver:	n/a	chr11:105728705-105728716
4	CEBPB	chr11:105675394-105675477	A549	lung:	n/a	chr11:105675400-105675411 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675411
5	CEBPB	chr11:105741354-105741697	HepG2	liver:	n/a	chr11:105741518-105741529
6	CEBPB	chr11:105773801-105774071	Hela-S3	cervix:	n/a	n/a
7	CEBPB	chr11:105755908-105756140	A549	lung:	n/a	chr11:105755995-105756006 chr11:105755997-105756008 chr11:105755995-105756008
8	CEBPB	chr11:105741409-105741609	Hela-S3	cervix:	n/a	chr11:105741518-105741529
9	CEBPB	chr11:105725537-105725836	IMR90	lung:	n/a	chr11:105725710-105725721
10	CEBPB	chr11:105725554-105725900	HepG2	liver:	n/a	chr11:105725710-105725721
11	CEBPB	chr11:105725578-105725909	A549	lung:	n/a	chr11:105725710-105725721
12	CEBPB	chr11:105773730-105774152	ECC-1	luminal epithelium:	n/a	n/a
13	CEBPB	chr11:105741407-105741690	IMR90	lung:	n/a	chr11:105741518-105741529
14	CEBPB	chr11:105675267-105675580	IMR90	lung:	n/a	chr11:105675400-105675411 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675409 chr11:105675398-105675411 chr11:105675398-105675411 chr11:105675400-105675409 chr11:105675400-105675411
15	CEBPB	chr11:105773693-105774202	ECC-1	luminal epithelium:	n/a	n/a
16	CEBPB	chr11:105728322-105728399	HepG2	liver:	n/a	n/a
17	CEBPB	chr11:105755861-105756129	HepG2	liver:	n/a	chr11:105755995-105756006 chr11:105755997-105756008 chr11:105755995-105756008
18	CEBPB	chr11:105719766-105719905	H1-hESC	embryonic stem cell:	n/a	n/a
19	CHD1	chr11:105738326-105738340	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr11:105732100-105732250	HFF	foreskin:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
21	CTCF	chr11:105733350-105734108	SK-N-SH	brain:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
22	CTCF	chr11:105687440-105687590	GM12874	blood:	n/a	n/a
23	CTCF	chr11:105732100-105732250	GM12873	blood:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
24	CTCF	chr11:105701860-105702010	NHEK	skin:	n/a	n/a
25	CTCF	chr11:105733620-105733770	AG04450	lung:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
26	CTCF	chr11:105733620-105733770	GM12874	blood:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
27	CTCF	chr11:105733620-105733770	HCT-116	colon:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
28	CTCF	chr11:105733680-105733830	HEK293	kidney:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
29	CTCF	chr11:105733580-105733730	SAEC	small airway:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
30	CTCF	chr11:105732036-105732204	SK-N-SH_RA	brain:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
31	CTCF	chr11:105707132-105707234	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr11:105707169-105707234	GM20000	blood:	n/a	n/a
33	CTCF	chr11:105732080-105732230	HCT-116	colon:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
34	CTCF	chr11:105732080-105732230	HRE	kidney:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
35	CTCF	chr11:105732083-105732225	GM12878	blood:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
36	CTCF	chr11:105733583-105733795	LNCaP	prostate:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
37	CTCF	chr11:105733620-105733770	HPF	lung:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
38	CTCF	chr11:105733357-105733959	HCT-116	colon:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
39	CTCF	chr11:105732061-105732212	HepG2	liver:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
40	CTCF	chr11:105733560-105733710	GM12872	blood:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
41	CTCF	chr11:105732080-105732230	HEEpiC	esophagus:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
42	CTCF	chr11:105733860-105734010	GM06990	blood:	n/a	n/a
43	CTCF	chr11:105698960-105699110	Caco-2	colon:	n/a	n/a
44	CTCF	chr11:105733640-105733790	HPAF	blood vessel:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
45	CTCF	chr11:105733313-105734125	A549	lung:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
46	CTCF	chr11:105732100-105732250	HCFaa	heart:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
47	CTCF	chr11:105733447-105733910	T-47D	breast:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
48	CTCF	chr11:105733620-105733770	HCFaa	heart:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707
49	CTCF	chr11:105732100-105732250	HA-sp	spinal cord:	n/a	chr11:105732146-105732153 chr11:105732134-105732155
50	CTCF	chr11:105733620-105733770	GM12872	blood:	n/a	chr11:105733691-105733709 chr11:105733696-105733704 chr11:105733692-105733708 chr11:105733686-105733707

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:105692831-105692881	ProgFib	skin:	n/a
2	chr11:105762374-105762424	HMEC	breast:	n/a
3	chr11:105692831-105692881	SK-N-SH_RA	brain:	n/a
4	chr11:105692831-105692881	AG10803	skin:	n/a
5	chr11:105762374-105762424	HEEpiC	esophagus:	n/a
6	chr11:105692831-105692881	BJ	skin:	n/a
7	chr11:105762374-105762424	HRPEpiC	eye:	n/a
8	chr11:105692831-105692881	AG04449	skin:	fetal
9	chr11:105762374-105762424	U87	brain:	n/a
10	chr11:105762374-105762424	ProgFib	skin:	n/a
11	chr11:105762374-105762424	ECC-1	luminal epithelium:	n/a
12	chr11:105692831-105692881	NH-A	brain:	n/a
13	chr11:105692831-105692881	IMR90	lung:	fetal
14	chr11:105692831-105692881	GM19239	blood:	n/a
15	chr11:105692831-105692881	HEK293	kidney:	embryo
16	chr11:105762374-105762424	Hepatocyte	liver:	n/a
17	chr11:105762374-105762424	PrEC	prostate:	n/a
18	chr11:105692831-105692881	Caco-2	colon:	n/a
19	chr11:105762374-105762424	PANC-1	pancreas:	n/a
20	chr11:105692831-105692881	AG04450	lung:	fetal
21	chr11:105762374-105762424	A549	lung:	n/a
22	chr11:105762374-105762424	HCPEpiC	choroid plexus:	n/a
23	chr11:105692831-105692881	BE2_C	brain:	n/a
24	chr11:105692831-105692881	CMK	blood:	n/a
25	chr11:105692831-105692881	HIPEpiC	eye:	n/a
26	chr11:105762374-105762424	AG09319	gingival:	n/a
27	chr11:105692831-105692881	GM12891	blood:	n/a
28	chr11:105692831-105692881	HCM	heart:	n/a
29	chr11:105692831-105692881	HPAEpiC	pulmonary alveolar:	n/a
30	chr11:105692831-105692881	AG09319	gingival:	n/a
31	chr11:105692831-105692881	SKMC	muscle:	n/a
32	chr11:105762374-105762424	HPAEpiC	pulmonary alveolar:	n/a
33	chr11:105692831-105692881	NT2-D1	testis:	n/a
34	chr11:105692831-105692881	Hepatocyte	liver:	n/a
35	chr11:105762374-105762424	HL-60	blood:	n/a
36	chr11:105692831-105692881	H1-hESC	embryonic stem cell:	embryo
37	chr11:105692831-105692881	HepG2	liver:	n/a
38	chr11:105762374-105762424	NHBE	bronchial:	n/a
39	chr11:105762374-105762424	HUVEC	blood vessel:	n/a
40	chr11:105762374-105762424	AG09309	skin:	n/a
41	chr11:105762374-105762424	HRCEpiC	kidney:	n/a
42	chr11:105762374-105762424	HepG2	liver:	n/a
43	chr11:105692831-105692881	PrEC	prostate:	n/a
44	chr11:105762374-105762424	BE2_C	brain:	n/a
45	chr11:105762374-105762424	GM06990	blood:	n/a
46	chr11:105692831-105692881	ovcar-3	ovarian:	n/a
47	chr11:105762374-105762424	SKMC	muscle:	n/a
48	chr11:105692831-105692881	GM06990	blood:	n/a
49	chr11:105762374-105762424	SK-N-MC	brain:	n/a
50	chr11:105692831-105692881	HCT-116	colon:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:103072545..103073152-chr11:105733681..105734257,2	MCF-7	breast:
2	chr11:105743815..105744316-chr12:94813536..94814043,2	MCF-7	breast:
3	chr11:103552695..103553725-chr11:105733540..105734127,3	MCF-7	breast:

Variant related genes	Relation type
GRIA4	TF binding region
RNU4-55P	TF binding region
GRIA4	CpG island
RNU4-55P	CpG island

Extended variants
information (count: 3429 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:3429 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3819071	chr11:105672706-105672707	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs573716010	chr11:105672763-105672764	ZNF genes & repeats Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs138449716	chr11:105672805-105672806	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs559456862	chr11:105672875-105672876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs141222371	chr11:105672947-105672948	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533245256	chr11:105672972-105672973	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs551837158	chr11:105673012-105673013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs150739658	chr11:105673015-105673016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529850200	chr11:105673021-105673022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs527785982	chr11:105673038-105673039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs630880	chr11:105673104-105673105	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs369282044	chr11:105673115-105673116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567863008	chr11:105673243-105673244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554756445	chr11:105673282-105673283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538026032	chr11:105673325-105673326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs549939836	chr11:105673358-105673359	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139065345	chr11:105673365-105673366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs538937877	chr11:105673393-105673394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557379404	chr11:105673401-105673402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs55888330	chr11:105673445-105673446	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs34574241	chr11:105673501-105673502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533898988	chr11:105673502-105673503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs397686666	chr11:105673508-105673509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs113729698	chr11:105673511-105673512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555137501	chr11:105673572-105673573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs182582340	chr11:105673635-105673636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573804906	chr11:105673720-105673721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114555697	chr11:105673731-105673732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs7358385	chr11:105673757-105673758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs73554208	chr11:105673827-105673828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs578030770	chr11:105673843-105673844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs545275657	chr11:105673873-105673874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs7358389	chr11:105673925-105673926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs11226853	chr11:105673939-105673940	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs527651312	chr11:105673966-105673967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs543128479	chr11:105673988-105673989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs186493815	chr11:105673996-105673997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561253295	chr11:105674007-105674008	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559572569	chr11:105674025-105674026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531816071	chr11:105674137-105674138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs528395226	chr11:105674241-105674242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs79419671	chr11:105674247-105674248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568267556	chr11:105674273-105674274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs532671749	chr11:105674290-105674291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547645324	chr11:105674312-105674313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566481109	chr11:105674326-105674327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs191046118	chr11:105674353-105674354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs72985188	chr11:105674363-105674364	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs555323995	chr11:105674416-105674417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs149459753	chr11:105674500-105674501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

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
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
Breast cancer	17142309	CNVD
Cancer	20164919	CNVD

Chromatin state (count:211 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:105658000-105689400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr11:105658200-105693200	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr11:105672600-105672800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr11:105672600-105672800	Enhancers	Brain Anterior Caudate	brain
5	chr11:105672600-105673000	Enhancers	Brain Cingulate Gyrus	brain
6	chr11:105686200-105686800	Enhancers	Fetal Muscle Leg	muscle
7	chr11:105687800-105692000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr11:105690800-105691400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr11:105690800-105692800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr11:105690800-105693400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr11:105691000-105692000	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr11:105691000-105693400	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr11:105691000-105693800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr11:105691200-105691400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr11:105691400-105691800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr11:105691400-105693400	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr11:105691400-105702000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr11:105691600-105692000	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr11:105691800-105692200	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr11:105691800-105693200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr11:105692000-105692400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chr11:105692000-105692800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr11:105692200-105692600	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr11:105692400-105692600	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr11:105692600-105692800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr11:105692600-105692800	Enhancers	Brain Inferior Temporal Lobe	brain
27	chr11:105692600-105693200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
28	chr11:105692600-105693400	Active TSS	ES-WA7 Cell Line	embryonic stem cell
29	chr11:105692800-105693400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr11:105692800-105693400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr11:105692800-105695200	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr11:105693200-105693400	Enhancers	Cortex derived primary cultured neurospheres	brain
33	chr11:105695200-105695800	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr11:105695600-105696000	Enhancers	Brain Substantia Nigra	brain
35	chr11:105699800-105700600	Enhancers	Primary B cells from peripheral blood	blood
36	chr11:105700000-105700400	Enhancers	GM12878-XiMat	blood
37	chr11:105700000-105700400	Enhancers	Monocytes-CD14+_RO01746	blood
38	chr11:105700000-105700600	Enhancers	Primary monocytes fromperipheralblood	blood
39	chr11:105700800-105701000	Enhancers	Pancreatic Islets	Pancreatic Islet
40	chr11:105702000-105703400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr11:105702800-105703200	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr11:105704800-105705400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr11:105705000-105705200	Enhancers	Breast Myoepithelial Primary Cells	Breast
44	chr11:105705000-105705600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr11:105705200-105764600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr11:105705400-105712800	Weak transcription	Cortex derived primary cultured neurospheres	brain
47	chr11:105709400-105709800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr11:105709400-105710000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr11:105709600-105709800	Enhancers	Hela-S3	cervix
50	chr11:105709600-105710000	Enhancers	NH-A	brain

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