Variant report

Variant	esv1815918
Chromosome Location	chr11:108900487-108948487
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:408)
CpG islands
(count:183)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:408 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr11:108911022-108911451	H1-hESC	embryonic stem cell:	n/a	n/a
2	ATF2	chr11:108910987-108911437	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr11:108914188-108914419	GM12878	blood:	n/a	n/a
4	BATF	chr11:108914217-108914418	GM12878	blood:	n/a	n/a
5	BCL11A	chr11:108914180-108914452	GM12878	blood:	n/a	chr11:108914250-108914259
6	CEBPB	chr11:108933263-108933534	HepG2	liver:	n/a	n/a
7	CEBPB	chr11:108933204-108933537	IMR90	lung:	n/a	n/a
8	CEBPB	chr11:108939447-108939579	K562	blood:	n/a	chr11:108939510-108939521
9	CEBPB	chr11:108906092-108906392	H1-hESC	embryonic stem cell:	n/a	chr11:108906201-108906212
10	CEBPB	chr11:108939439-108939612	HepG2	liver:	n/a	chr11:108939510-108939521
11	CEBPB	chr11:108906187-108906219	HepG2	liver:	n/a	chr11:108906201-108906212
12	CEBPB	chr11:108918761-108919039	IMR90	lung:	n/a	chr11:108918880-108918891 chr11:108918878-108918891 chr11:108918880-108918891
13	CREB1	chr11:108911088-108911360	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr11:108911075-108911368	HepG2	liver:	n/a	n/a
15	CTCF	chr11:108909240-108909390	AG09319	gingival:	n/a	n/a
16	CTCF	chr11:108909229-108909468	NHEK	skin:	n/a	n/a
17	CTCF	chr11:108911070-108911393	K562	blood:	n/a	n/a
18	CTCF	chr11:108911048-108911331	K562	blood:	n/a	n/a
19	CTCF	chr11:108911180-108911330	HCT-116	colon:	n/a	n/a
20	CTCF	chr11:108911150-108911275	ProgFib	skin:	n/a	n/a
21	CTCF	chr11:108911242-108911285	Pancreas_OC	pancreas:	n/a	n/a
22	CTCF	chr11:108911181-108911252	GM10266	blood:	n/a	n/a
23	CTCF	chr11:108911139-108911320	GM12891	blood:	n/a	n/a
24	CTCF	chr11:108909200-108909350	HMEC	breast:	n/a	n/a
25	CTCF	chr11:108911140-108911290	WERI-Rb-1	eye:	n/a	n/a
26	CTCF	chr11:108911175-108911253	HUVEC	blood vessel:	n/a	n/a
27	CTCF	chr11:108909300-108909450	HMF	breast:	n/a	n/a
28	CTCF	chr11:108911120-108911270	HUVEC	blood vessel:	n/a	n/a
29	CTCF	chr11:108911193-108911258	GM20000	blood:	n/a	n/a
30	CTCF	chr11:108911122-108911326	GM12892	blood:	n/a	n/a
31	CTCF	chr11:108911140-108911290	NB4	blood:	n/a	n/a
32	CTCF	chr11:108911143-108911311	GM19239	blood:	n/a	n/a
33	CTCF	chr11:108911140-108911290	HA-sp	spinal cord:	n/a	n/a
34	CTCF	chr11:108911073-108911393	GM12878	blood:	n/a	n/a
35	CTCF	chr11:108911160-108911310	HRPEpiC	eye:	n/a	n/a
36	CTCF	chr11:108911157-108911268	LNCaP	prostate:	n/a	n/a
37	CTCF	chr11:108942460-108942610	NHLF	lung:	n/a	n/a
38	CTCF	chr11:108911140-108911290	SAEC	small airway:	n/a	n/a
39	CTCF	chr11:108911180-108911330	HFF-Myc	foreskin:	n/a	n/a
40	CTCF	chr11:108911200-108911350	HPAF	blood vessel:	n/a	n/a
41	CTCF	chr11:108924043-108924098	GM20000	blood:	n/a	n/a
42	CTCF	chr11:108911157-108911275	Fibrobl	skin:	n/a	n/a
43	CTCF	chr11:108909240-108909390	HCM	heart:	n/a	n/a
44	CTCF	chr11:108909220-108909370	AG09309	skin:	n/a	n/a
45	CTCF	chr11:108911118-108911322	GM12878	blood:	n/a	n/a
46	CTCF	chr11:108911160-108911310	HMF	breast:	n/a	n/a
47	CTCF	chr11:108911017-108911380	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr11:108911033-108911355	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr11:108911195-108911275	GM13977	blood:	n/a	n/a
50	CTCF	chr11:108911123-108911317	HepG2	liver:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:108906099-108906149	HEEpiC	esophagus:	n/a
2	chr11:108906099-108906149	NHBE	bronchial:	n/a
3	chr11:108918285-108918335	Caco-2	colon:	n/a
4	chr11:108909215-108909265	IMR90	lung:	fetal
5	chr11:108909215-108909265	AG09309	skin:	n/a
6	chr11:108906099-108906149	AG09319	gingival:	n/a
7	chr11:108918285-108918335	AG10803	skin:	n/a
8	chr11:108906099-108906149	U87	brain:	n/a
9	chr11:108906099-108906149	Hela-S3	cervix:	n/a
10	chr11:108918285-108918335	GM06990	blood:	n/a
11	chr11:108906099-108906149	ECC-1	luminal epithelium:	n/a
12	chr11:108906099-108906149	RPTEC	kidney:	n/a
13	chr11:108906099-108906149	T-47D	breast:	n/a
14	chr11:108909215-108909265	MCF-7	breast:	n/a
15	chr11:108906099-108906149	HL-60	blood:	n/a
16	chr11:108909215-108909265	LNCaP	prostate:	n/a
17	chr11:108918285-108918335	HPAEpiC	pulmonary alveolar:	n/a
18	chr11:108909215-108909265	HepG2	liver:	n/a
19	chr11:108906099-108906149	HUVEC	blood vessel:	n/a
20	chr11:108918285-108918335	IMR90	lung:	fetal
21	chr11:108909215-108909265	ProgFib	skin:	n/a
22	chr11:108909215-108909265	PrEC	prostate:	n/a
23	chr11:108918285-108918335	GM12891	blood:	n/a
24	chr11:108918285-108918335	SK-N-MC	brain:	n/a
25	chr11:108909215-108909265	AoSMC	blood vessel:	n/a
26	chr11:108909215-108909265	Caco-2	colon:	n/a
27	chr11:108918285-108918335	HEEpiC	esophagus:	n/a
28	chr11:108918285-108918335	Jurkat	blood:	n/a
29	chr11:108918285-108918335	HEK293	kidney:	embryo
30	chr11:108906099-108906149	HIPEpiC	eye:	n/a
31	chr11:108906099-108906149	AG04449	skin:	fetal
32	chr11:108918285-108918335	HCM	heart:	n/a
33	chr11:108918285-108918335	Hela-S3	cervix:	n/a
34	chr11:108909215-108909265	HIPEpiC	eye:	n/a
35	chr11:108906099-108906149	LNCaP	prostate:	n/a
36	chr11:108918285-108918335	HIPEpiC	eye:	n/a
37	chr11:108906099-108906149	AG10803	skin:	n/a
38	chr11:108909215-108909265	SKMC	muscle:	n/a
39	chr11:108906099-108906149	AG09309	skin:	n/a
40	chr11:108909215-108909265	GM12878	blood:	n/a
41	chr11:108918285-108918335	HMEC	breast:	n/a
42	chr11:108906099-108906149	PANC-1	pancreas:	n/a
43	chr11:108906099-108906149	HRPEpiC	eye:	n/a
44	chr11:108909215-108909265	U87	brain:	n/a
45	chr11:108909215-108909265	NHBE	bronchial:	n/a
46	chr11:108918285-108918335	HRPEpiC	eye:	n/a
47	chr11:108918285-108918335	NT2-D1	testis:	n/a
48	chr11:108906099-108906149	PrEC	prostate:	n/a
49	chr11:108909215-108909265	HL-60	blood:	n/a
50	chr11:108906099-108906149	AoSMC	blood vessel:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
2	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
3	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
4	chr11:108927357..108928938-chr11:108932482..108934210,2	K562	blood:
5	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:
6	chr11:108873859..108875938-chr11:108935111..108937056,2	K562	blood:
7	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
8	chr11:108905168..108907464-chr11:108909151..108912288,3	K562	blood:
9	chr11:108899961..108902009-chr11:108909481..108912314,2	K562	blood:
10	chr11:108936870..108939701-chr11:108941192..108943026,2	K562	blood:
11	chr11:108905323..108906917-chr11:108910788..108913428,2	K562	blood:

(count:1 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXPH5-1	chr11:108908470-108908694	ENSG00000255528

No data

Variant related genes	Relation type
ENSG00000255528	TF binding region
ENSG00000255528	CpG island

Extended variants
information (count: 1769 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549465200	chr11:108900505-108900506	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs1509710	chr11:108900583-108900584	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs150125068	chr11:108900599-108900600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs145514330	chr11:108900635-108900636	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs565841520	chr11:108900665-108900666	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs536567924	chr11:108900684-108900685	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs369433629	chr11:108900688-108900689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs565416097	chr11:108900706-108900707	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554864367	chr11:108900735-108900736	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs373104317	chr11:108900746-108900747	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148970543	chr11:108900795-108900796	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2136531	chr11:108900805-108900806	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
13	rs143771693	chr11:108900845-108900846	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs61344275	chr11:108900849-108900850	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs201027781	chr11:108900874-108900875	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1509708	chr11:108900875-108900876	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs138462606	chr11:108900933-108900934	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs1509707	chr11:108900947-108900948	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs185353469	chr11:108900952-108900953	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143088671	chr11:108900962-108900963	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs549549369	chr11:108900987-108900988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199551600	chr11:108901049-108901050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs144969289	chr11:108901051-108901052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs370315303	chr11:108901057-108901058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs532133243	chr11:108901064-108901065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs547436823	chr11:108901073-108901074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs11212864	chr11:108901120-108901121	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs550401950	chr11:108901160-108901161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76650356	chr11:108901171-108901172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs536406264	chr11:108901173-108901174	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs78473768	chr11:108901178-108901179	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs11212865	chr11:108901192-108901193	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs71475114	chr11:108901193-108901194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs80311405	chr11:108901195-108901196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs111805567	chr11:108901196-108901197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76468134	chr11:108901203-108901204	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556311146	chr11:108901214-108901215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs577940659	chr11:108901215-108901216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111888157	chr11:108901266-108901267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs10749934	chr11:108901267-108901268	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs188683339	chr11:108901282-108901283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs193286674	chr11:108901284-108901285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77162791	chr11:108901287-108901288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184310906	chr11:108901304-108901305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs561134993	chr11:108901307-108901308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs111384475	chr11:108901310-108901311	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544068411	chr11:108901329-108901330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs180882291	chr11:108901336-108901337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201987847	chr11:108901348-108901349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374215781	chr11:108901355-108901356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:93)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	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
Chronic lymphocytic leukemia	21546498	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
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
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
Prostate cancer	18632612	CNVD
Renal cell carcinoma	21668985	CNVD
Cancer	20164920	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21509527	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:252 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:108894200-108903800	Weak transcription	Osteobl	bone
2	chr11:108899000-108904200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr11:108899200-108900600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr11:108899800-108901000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr11:108900600-108900800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr11:108900600-108901000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr11:108900800-108901400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr11:108901000-108904000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr11:108901000-108908800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr11:108901400-108902000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr11:108901600-108901800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr11:108901600-108902000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr11:108901600-108902000	Enhancers	HMEC	breast
14	chr11:108901600-108902200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr11:108901800-108902200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr11:108901800-108902200	Enhancers	NHEK	skin
17	chr11:108901800-108904800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr11:108902000-108904400	Weak transcription	HMEC	breast
19	chr11:108902000-108904600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr11:108902200-108904600	Weak transcription	NHEK	skin
21	chr11:108902600-108905800	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr11:108902800-108903600	Enhancers	HUVEC	blood vessel
23	chr11:108903400-108904600	Enhancers	NH-A	brain
24	chr11:108903600-108904600	Weak transcription	HUVEC	blood vessel
25	chr11:108903800-108904800	Enhancers	Osteobl	bone
26	chr11:108904000-108904800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr11:108904000-108906000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr11:108904200-108905400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
29	chr11:108904400-108905600	Enhancers	HMEC	breast
30	chr11:108904600-108905000	Flanking Active TSS	NHEK	skin
31	chr11:108904600-108905400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr11:108904600-108905400	Enhancers	HSMMtube	muscle
33	chr11:108904600-108905400	Flanking Active TSS	NH-A	brain
34	chr11:108904600-108905600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr11:108904600-108906400	Enhancers	HUVEC	blood vessel
36	chr11:108904800-108905400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr11:108904800-108905400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr11:108904800-108905400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr11:108904800-108905400	Enhancers	NHDF-Ad	bronchial
40	chr11:108904800-108905400	Flanking Active TSS	Osteobl	bone
41	chr11:108904800-108905600	Enhancers	HSMM	muscle
42	chr11:108904800-108906000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr11:108905000-108905400	Enhancers	NHLF	lung
44	chr11:108905000-108905600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr11:108905000-108905600	Enhancers	NHEK	skin
46	chr11:108905000-108906600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
47	chr11:108905200-108905600	Enhancers	Brain Anterior Caudate	brain
48	chr11:108905400-108906000	Enhancers	Muscle Satellite Cultured Cells	--
49	chr11:108905400-108907400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr11:108905400-108907600	Enhancers	NH-A	brain

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