Variant report

Variant	esv32703
Chromosome Location	chr11:65213860-65222026
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	chr11:65216931-65216935	K562	blood:	n/a	n/a
2	BCL3	chr11:65215465-65216445	A549	lung:	n/a	chr11:65216106-65216115
3	BCL3	chr11:65215597-65215975	A549	lung:	n/a	n/a
4	CBX3	chr11:65216008-65216553	K562	blood:	n/a	n/a
5	CEBPB	chr11:65220851-65221040	HepG2	liver:	n/a	n/a
6	CEBPB	chr11:65220654-65221095	IMR90	lung:	n/a	n/a
7	CEBPB	chr11:65220554-65221095	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr11:65220098-65220215	A549	lung:	n/a	chr11:65220109-65220120
9	CEBPB	chr11:65220587-65221168	A549	lung:	n/a	n/a
10	CEBPB	chr11:65220779-65221018	K562	blood:	n/a	n/a
11	CEBPB	chr11:65220716-65221040	A549	lung:	n/a	n/a
12	CEBPB	chr11:65220045-65220245	HepG2	liver:	n/a	chr11:65220109-65220120
13	CEBPB	chr11:65220800-65221053	K562	blood:	n/a	n/a
14	CEBPB	chr11:65220089-65220236	Hela-S3	cervix:	n/a	chr11:65220109-65220120
15	CEBPB	chr11:65220702-65221060	A549	lung:	n/a	n/a
16	CHD1	chr11:65221247-65223345	IMR90	lung:	n/a	n/a
17	CHD1	chr11:65183014-65218224	IMR90	lung:	n/a	chr11:65189696-65189706 chr11:65213009-65213016
18	CHD2	chr11:65213310-65214465	HepG2	liver:	n/a	n/a
19	CHD2	chr11:65220624-65220830	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr11:65216315-65216421	K562	blood:	n/a	n/a
21	CHD2	chr11:65212650-65214510	K562	blood:	n/a	chr11:65213009-65213016
22	CHD2	chr11:65215705-65216974	HepG2	liver:	n/a	n/a
23	CTCF	chr11:65216100-65216250	NHDF-neo	bronchial:	n/a	chr11:65216197-65216210
24	CTCF	chr11:65216240-65216390	HEEpiC	esophagus:	n/a	chr11:65216352-65216361
25	CTCF	chr11:65216220-65216370	HCM	heart:	n/a	chr11:65216352-65216361
26	CTCF	chr11:65216160-65216310	HMEC	breast:	n/a	chr11:65216197-65216210
27	CTCF	chr11:65216220-65216370	AG10803	skin:	n/a	chr11:65216352-65216361
28	CTCF	chr11:65216100-65216250	AG04449	skin:	n/a	chr11:65216197-65216210
29	CTCF	chr11:65216100-65216250	Caco-2	colon:	n/a	chr11:65216197-65216210
30	CTCF	chr11:65216080-65216230	AG04449	skin:	n/a	chr11:65216197-65216210
31	CTCF	chr11:65216100-65216250	HPAF	blood vessel:	n/a	chr11:65216197-65216210
32	CTCF	chr11:65216120-65216270	HBMEC	blood vessel:	n/a	chr11:65216197-65216210
33	CTCF	chr11:65216100-65216250	NHEK	skin:	n/a	chr11:65216197-65216210
34	CTCF	chr11:65216100-65216250	HCM	heart:	n/a	chr11:65216197-65216210
35	CTCF	chr11:65216080-65216230	SAEC	small airway:	n/a	chr11:65216197-65216210
36	CTCF	chr11:65216100-65216250	HCFaa	heart:	n/a	chr11:65216197-65216210
37	CTCF	chr11:65216200-65216350	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr11:65216140-65216290	Hela-S3	cervix:	n/a	chr11:65216197-65216210
39	CTCF	chr11:65216140-65216290	HA-sp	spinal cord:	n/a	chr11:65216197-65216210
40	CTCF	chr11:65216080-65216230	AG10803	skin:	n/a	chr11:65216197-65216210
41	CTCF	chr11:65215720-65215870	GM12866	blood:	n/a	n/a
42	CTCF	chr11:65216200-65216350	HRPEpiC	eye:	n/a	n/a
43	CTCF	chr11:65216180-65216330	HBMEC	blood vessel:	n/a	chr11:65216197-65216210
44	CTCF	chr11:65216040-65216190	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr11:65216020-65216170	NHLF	lung:	n/a	n/a
46	CTCF	chr11:65214360-65214510	HCPEpiC	choroid plexus:	n/a	chr11:65214370-65214383
47	CTCFL	chr11:65216154-65216394	K562	blood:	n/a	n/a
48	CUX1	chr11:65216293-65216356	K562	blood:	n/a	n/a
49	E2F4	chr11:65220641-65221077	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr11:65215653-65215927	MCF10A-Er-Src	breast:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:17230936..17232850-chr11:65213423..65216016,2	K562	blood:
2	chr11:33757459..33757967-chr11:65216081..65217053,2	Hela-S3	cervix:
3	chr11:65122004..65123879-chr11:65220475..65223059,2	K562	blood:
4	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
5	chr11:62608095..62609669-chr11:65220631..65223111,2	MCF-7	breast:
6	chr11:65178877..65218546-chr11:65218612..65286191,1014	K562	blood:
7	chr11:65184008..65184518-chr11:65215992..65216526,2	MCF-7	breast:
8	chr11:65042714..65044307-chr11:65213952..65215856,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AP000769.1-1	chr11:65219924-65221119	NONHSAT022120
2	lnc-AP000769.1-1	chr11:65218531-65218571	NONHSAT022120

Variant related genes	Relation type
ENSG00000173727	TF binding region
ENSG00000272426	chromatin interactions
ENSG00000270526	chromatin interactions
ENSG00000173825	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000085063	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000173727	chromatin interactions

Extended variants
information (count: 357 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:357 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183646687	chr11:65213912-65213913	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs577842445	chr11:65213965-65213966	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs538422567	chr11:65213975-65213976	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs138083707	chr11:65214064-65214065	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
5	rs554081972	chr11:65214079-65214080	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
6	rs76653598	chr11:65214125-65214126	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
7	rs572690700	chr11:65214137-65214138	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
8	rs544749856	chr11:65214141-65214142	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
9	rs562958931	chr11:65214185-65214186	Genic enhancers Strong transcription Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
10	rs189244194	chr11:65214249-65214250	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
11	rs79890463	chr11:65214257-65214258	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
12	rs192884082	chr11:65214258-65214259	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
13	rs564589606	chr11:65214286-65214287	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs142685892	chr11:65214299-65214300	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs547711270	chr11:65214319-65214320	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs561172839	chr11:65214349-65214350	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs529653731	chr11:65214404-65214405	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs530536480	chr11:65214453-65214454	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs369484034	chr11:65214501-65214502	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs543827591	chr11:65214538-65214539	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs538331287	chr11:65214566-65214567	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs183793440	chr11:65214575-65214576	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs564030702	chr11:65214578-65214579	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs571496103	chr11:65214582-65214583	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs80310681	chr11:65214583-65214584	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs371747004	chr11:65214599-65214600	Strong transcription Genic enhancers Weak transcription Enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs527326144	chr11:65214608-65214609	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs145930298	chr11:65214659-65214660	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs139806173	chr11:65214707-65214708	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs187075023	chr11:65214714-65214715	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs549690619	chr11:65214715-65214716	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs191675884	chr11:65214741-65214742	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
33	rs576418349	chr11:65214754-65214755	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
34	rs545162058	chr11:65214777-65214778	Strong transcription Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
35	rs559140864	chr11:65214815-65214816	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
36	rs551962503	chr11:65214883-65214884	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
37	rs142077783	chr11:65214898-65214899	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs566324133	chr11:65214946-65214947	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs150741855	chr11:65215020-65215021	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs77445997	chr11:65215109-65215110	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs111949562	chr11:65215110-65215111	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs528650616	chr11:65215120-65215121	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs529968698	chr11:65215129-65215130	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs570593135	chr11:65215185-65215186	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs184227009	chr11:65215219-65215220	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs563120800	chr11:65215306-65215307	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs532171183	chr11:65215308-65215309	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs139096589	chr11:65215322-65215323	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs150023004	chr11:65215345-65215346	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs112217205	chr11:65215350-65215351	Weak transcription Genic enhancers Strong transcription Enhancers	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Multiple myeloma	20724749	CNVD
Wilms tumour	21544195	CNVD
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:65198000-65216000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr11:65200600-65214200	Strong transcription	NH-A	brain
3	chr11:65202600-65214400	Genic enhancers	A549	lung
4	chr11:65205200-65214400	Genic enhancers	Placenta	Placenta
5	chr11:65205600-65214800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr11:65205600-65217600	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr11:65206600-65214400	Genic enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr11:65206600-65222000	Weak transcription	Fetal Kidney	kidney
9	chr11:65207800-65214600	Genic enhancers	NHLF	lung
10	chr11:65208200-65214600	Genic enhancers	Adipose Nuclei	Adipose
11	chr11:65208600-65214400	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin02	Skin
12	chr11:65208800-65214200	Strong transcription	Duodenum Smooth Muscle	Duodenum
13	chr11:65209000-65217400	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr11:65209200-65214400	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr11:65209200-65214400	Genic enhancers	Fetal Muscle Leg	muscle
16	chr11:65209400-65214200	Genic enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr11:65209400-65214400	Strong transcription	Thymus	Thymus
18	chr11:65209400-65214400	Genic enhancers	Spleen	Spleen
19	chr11:65209400-65214600	Genic enhancers	Fetal Muscle Trunk	muscle
20	chr11:65209600-65214600	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr11:65209600-65214600	Genic enhancers	NHDF-Ad	bronchial
22	chr11:65209800-65214000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr11:65210000-65222000	Weak transcription	Brain Angular Gyrus	brain
24	chr11:65210000-65222200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr11:65210200-65214600	Strong transcription	Fetal Intestine Large	intestine
26	chr11:65210400-65216200	Genic enhancers	Muscle Satellite Cultured Cells	--
27	chr11:65210800-65214200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
28	chr11:65210800-65214800	Strong transcription	Fetal Intestine Small	intestine
29	chr11:65210800-65222000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr11:65211000-65214600	Transcr. at gene 5' and 3'	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr11:65211000-65214600	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
32	chr11:65211200-65220000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr11:65211400-65214000	Weak transcription	HSMMtube	muscle
34	chr11:65211400-65214600	Strong transcription	Left Ventricle	heart
35	chr11:65211400-65222000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
36	chr11:65211600-65214200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
37	chr11:65211600-65214400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr11:65211600-65214400	Strong transcription	Brain Cingulate Gyrus	brain
39	chr11:65211600-65214600	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr11:65211600-65214600	Strong transcription	Fetal Stomach	stomach
41	chr11:65211600-65214600	Strong transcription	Ovary	ovary
42	chr11:65211600-65214600	Strong transcription	Rectal Mucosa Donor 31	rectum
43	chr11:65211600-65214600	Genic enhancers	Skeletal Muscle Male	skeletal muscle
44	chr11:65211600-65221800	Weak transcription	HUVEC	blood vessel
45	chr11:65212000-65214400	Strong transcription	Colonic Mucosa	Colon
46	chr11:65212200-65214200	Strong transcription	Lung	lung
47	chr11:65212200-65214200	Enhancers	GM12878-XiMat	blood
48	chr11:65212200-65214600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr11:65212200-65214600	Strong transcription	Right Ventricle	heart
50	chr11:65212200-65214800	Strong transcription	Brain Hippocampus Middle	brain

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