Variant report

Variant	nsv1041081
Chromosome Location	chr11:104797775-104912458
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1256)
CpG islands
(count:1525)
Chromatin interactive
region (count:5)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:2)

(count:1256 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr11:104838864-104839516	HepG2	liver:	n/a	n/a
2	ARID3A	chr11:104870648-104871335	HepG2	liver:	n/a	n/a
3	ARID3A	chr11:104874651-104875141	HepG2	liver:	n/a	n/a
4	ARID3A	chr11:104817646-104818039	HepG2	liver:	n/a	n/a
5	ARID3A	chr11:104814897-104815170	HepG2	liver:	n/a	n/a
6	ARID3A	chr11:104865690-104866388	HepG2	liver:	n/a	n/a
7	ARID3A	chr11:104838331-104838340	HepG2	liver:	n/a	n/a
8	ARID3A	chr11:104814360-104814630	HepG2	liver:	n/a	n/a
9	ARID3A	chr11:104855516-104855852	HepG2	liver:	n/a	n/a
10	ARID3A	chr11:104827306-104827643	HepG2	liver:	n/a	n/a
11	BATF	chr11:104905693-104906006	GM12878	blood:	n/a	n/a
12	BATF	chr11:104905695-104905944	GM12878	blood:	n/a	n/a
13	BHLHE40	chr11:104885004-104885054	GM12878	blood:	n/a	n/a
14	BHLHE40	chr11:104871511-104871851	GM12878	blood:	n/a	n/a
15	BHLHE40	chr11:104865796-104866149	HepG2	liver:	n/a	n/a
16	BHLHE40	chr11:104840122-104840539	HepG2	liver:	n/a	n/a
17	BHLHE40	chr11:104838963-104839549	GM12878	blood:	n/a	n/a
18	BRCA1	chr11:104839197-104839617	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr11:104838120-104838701	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr11:104839210-104839268	HepG2	liver:	n/a	n/a
21	CBX3	chr11:104817608-104818133	HCT-116	colon:	n/a	n/a
22	CBX3	chr11:104871491-104872014	HCT-116	colon:	n/a	n/a
23	CBX3	chr11:104843718-104843957	HCT-116	colon:	n/a	n/a
24	CEBPB	chr11:104839191-104839496	HepG2	liver:	n/a	n/a
25	CEBPB	chr11:104827282-104827644	IMR90	lung:	n/a	chr11:104827468-104827479
26	CEBPB	chr11:104874820-104875056	A549	lung:	n/a	chr11:104874861-104874874 chr11:104874861-104874872 chr11:104874862-104874873
27	CEBPB	chr11:104874739-104875152	Hela-S3	cervix:	n/a	chr11:104874861-104874874 chr11:104874861-104874872 chr11:104875128-104875139 chr11:104874862-104874873
28	CEBPB	chr11:104855556-104855922	HepG2	liver:	n/a	chr11:104855728-104855739
29	CEBPB	chr11:104827075-104827789	HCT-116	colon:	n/a	chr11:104827468-104827479
30	CEBPB	chr11:104837727-104839837	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr11:104814346-104815203	HepG2	liver:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
32	CEBPB	chr11:104905287-104906325	Hela-S3	cervix:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
33	CEBPB	chr11:104868523-104868706	IMR90	lung:	n/a	n/a
34	CEBPB	chr11:104827214-104827637	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
35	CEBPB	chr11:104827216-104827712	HCT-116	colon:	n/a	chr11:104827468-104827479
36	CEBPB	chr11:104905228-104906180	IMR90	lung:	n/a	chr11:104905915-104905932 chr11:104905600-104905613 chr11:104905919-104905930
37	CEBPB	chr11:104840644-104840840	HepG2	liver:	n/a	n/a
38	CEBPB	chr11:104858927-104859103	HepG2	liver:	n/a	chr11:104858982-104858993
39	CEBPB	chr11:104838936-104839546	A549	lung:	n/a	n/a
40	CEBPB	chr11:104827299-104827601	HepG2	liver:	n/a	chr11:104827468-104827479
41	CEBPB	chr11:104875690-104876153	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr11:104827300-104827618	K562	blood:	n/a	chr11:104827468-104827479
43	CEBPB	chr11:104817693-104817982	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr11:104827192-104827735	A549	lung:	n/a	chr11:104827468-104827479
45	CEBPB	chr11:104865865-104866257	HepG2	liver:	n/a	chr11:104866094-104866106
46	CEBPB	chr11:104839158-104839571	MCF-7	breast:	n/a	n/a
47	CEBPB	chr11:104827200-104827640	ECC-1	luminal epithelium:	n/a	chr11:104827468-104827479
48	CEBPB	chr11:104814361-104814678	IMR90	lung:	n/a	chr11:104814576-104814588 chr11:104814528-104814541 chr11:104814528-104814541 chr11:104814528-104814539 chr11:104814529-104814540
49	CEBPB	chr11:104839098-104839568	IMR90	lung:	n/a	n/a
50	CEBPB	chr11:104871581-104872704	Hela-S3	cervix:	n/a	n/a

(count:1525 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104912363-104912413	HL-60	blood:	n/a
2	chr11:104887371-104887421	PFSK-1	brain:	n/a
3	chr11:104840183-104840233	HCF	heart:	n/a
4	chr11:104865951-104866001	K562	blood:	n/a
5	chr11:104871117-104871167	BJ	skin:	n/a
6	chr11:104871117-104871167	GM06990	blood:	n/a
7	chr11:104839343-104839393	MCF10A-Er-Src	breast:	n/a
8	chr11:104839343-104839393	BJ	skin:	n/a
9	chr11:104827790-104827840	A549	lung:	n/a
10	chr11:104839343-104839393	K562	blood:	n/a
11	chr11:104905834-104905884	GM06990	blood:	n/a
12	chr11:104840183-104840233	HEEpiC	esophagus:	n/a
13	chr11:104828060-104828110	HRE	kidney:	n/a
14	chr11:104839343-104839393	SK-N-MC	brain:	n/a
15	chr11:104817914-104817964	HIPEpiC	eye:	n/a
16	chr11:104906381-104906431	HRPEpiC	eye:	n/a
17	chr11:104871117-104871167	SAEC	small airway:	n/a
18	chr11:104871117-104871167	MCF10A-Er-Src	breast:	n/a
19	chr11:104827238-104827288	HEK293	kidney:	embryo
20	chr11:104827790-104827840	PANC-1	pancreas:	n/a
21	chr11:104814390-104814440	ECC-1	luminal epithelium:	n/a
22	chr11:104912363-104912413	T-47D	breast:	n/a
23	chr11:104839281-104839331	SK-N-SH	brain:	n/a
24	chr11:104896587-104896637	MCF10A-Er-Src	breast:	n/a
25	chr11:104839349-104839399	T-47D	breast:	n/a
26	chr11:104871117-104871167	ovcar-3	ovarian:	n/a
27	chr11:104814390-104814440	NHBE	bronchial:	n/a
28	chr11:104879683-104879733	Hela-S3	cervix:	n/a
29	chr11:104840183-104840233	T-47D	breast:	n/a
30	chr11:104906381-104906431	HIPEpiC	eye:	n/a
31	chr11:104906381-104906431	AG04449	skin:	fetal
32	chr11:104827790-104827840	ovcar-3	ovarian:	n/a
33	chr11:104894514-104894564	SKMC	muscle:	n/a
34	chr11:104839349-104839399	BE2_C	brain:	n/a
35	chr11:104906381-104906431	AG10803	skin:	n/a
36	chr11:104865951-104866001	AG04450	lung:	fetal
37	chr11:104876060-104876110	CMK	blood:	n/a
38	chr11:104839074-104839124	GM19239	blood:	n/a
39	chr11:104907029-104907079	ProgFib	skin:	n/a
40	chr11:104906381-104906431	GM12892	blood:	n/a
41	chr11:104896587-104896637	NHBE	bronchial:	n/a
42	chr11:104879683-104879733	HRPEpiC	eye:	n/a
43	chr11:104907029-104907079	A549	lung:	n/a
44	chr11:104865951-104866001	NH-A	brain:	n/a
45	chr11:104906381-104906431	AG09309	skin:	n/a
46	chr11:104839281-104839331	HCPEpiC	choroid plexus:	n/a
47	chr11:104906381-104906431	ProgFib	skin:	n/a
48	chr11:104905889-104905939	HRCEpiC	kidney:	n/a
49	chr11:104839343-104839393	GM06990	blood:	n/a
50	chr11:104828060-104828110	AoSMC	blood vessel:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:
2	chr11:104838939..104839536-chr7:127228342..127228894,2	Hela-S3	cervix:
3	chr11:104894289..104896311-chr11:104901290..104902903,2	K562	blood:
4	chr1:151511788..151512678-chr11:104838165..104838828,2	Hela-S3	cervix:
5	chr11:62420312..62421283-chr11:104838756..104839379,2	Hela-S3	cervix:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP4-1	chr11:104817810-104818085	NONHSAT023946
2	lnc-CASP5-2	chr11:104897569-104897899	NONHSAT023949
3	lnc-CARD16-1	chr11:104904935-104905085	NONHSAT023950
4	lnc-CARD16-1	chr11:104901581-104902007	NONHSAT023950
5	lnc-CASP4-1	chr11:104815475-104815578	NONHSAT023946
6	lnc-CASP4-1	chr11:104819260-104819461	NONHSAT023947
7	lnc-CASP4-1	chr11:104817351-104817919	NONHSAT023947
8	lnc-CASP4-1	chr11:104813600-104813700	NONHSAT023946
9	lnc-CASP5-2	chr11:104896235-104896327	NONHSAT023949

No data

(count:2 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CASP4	hsa-miR-26b-5p	chr11:104822275-104822295
2	CASP4	hsa-miR-26b-5p	chr11:104822249-104822272

Variant related genes	Relation type
CASP1	TF binding region
CASP5	TF binding region
CASP4	TF binding region
CASP1	CpG island
CASP5	CpG island
CASP4	CpG island
ENSG00000004059	chromatin interactions
ENSG00000185085	chromatin interactions

Extended variants
information (count: 4003 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:4003 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs180797996	chr11:104797791-104797792	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs115283099	chr11:104797796-104797797	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs548182	chr11:104797862-104797863	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs371265350	chr11:104797901-104797902	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs870402	chr11:104797918-104797919	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs80088976	chr11:104797919-104797920	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs185017700	chr11:104797927-104797928	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs573707948	chr11:104797928-104797929	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs189444037	chr11:104797933-104797934	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs10791738	chr11:104797957-104797958	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs181870801	chr11:104798048-104798049	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544635005	chr11:104798051-104798052	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs111419940	chr11:104798086-104798087	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs564526498	chr11:104798087-104798088	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs533488268	chr11:104798091-104798092	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs550202107	chr11:104798092-104798093	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs35285842	chr11:104798101-104798102	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs186824412	chr11:104798129-104798130	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs545491	chr11:104798145-104798146	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs117248204	chr11:104798153-104798154	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs566150422	chr11:104798195-104798196	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs552060489	chr11:104798229-104798230	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551833109	chr11:104798244-104798245	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571280644	chr11:104798284-104798285	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149264803	chr11:104798290-104798291	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35248723	chr11:104798296-104798297	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537355356	chr11:104798325-104798326	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556937118	chr11:104798328-104798329	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs114929430	chr11:104798331-104798332	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536034176	chr11:104798370-104798371	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs562177542	chr11:104798391-104798392	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs191208834	chr11:104798410-104798411	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs12792277	chr11:104798416-104798417	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs376511045	chr11:104798418-104798419	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs542762	chr11:104798458-104798459	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs564581554	chr11:104798491-104798492	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs574843995	chr11:104798494-104798495	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs181184670	chr11:104798535-104798536	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs7926199	chr11:104798545-104798546	Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
40	rs529510514	chr11:104798587-104798588	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs11226562	chr11:104803226-104803227	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs149002485	chr11:104803272-104803273	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs538527881	chr11:104803273-104803274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs116517548	chr11:104803329-104803330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs113249420	chr11:104803394-104803395	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs181091231	chr11:104803397-104803398	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs533922138	chr11:104803429-104803430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs148145277	chr11:104803493-104803494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs528023926	chr11:104803515-104803516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547635281	chr11:104803536-104803537	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
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
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:2005 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104797200-104798400	Enhancers	Dnd41	blood
2	chr11:104797600-104797800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr11:104797600-104798000	Enhancers	Fetal Muscle Leg	muscle
4	chr11:104797600-104798200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr11:104797600-104798400	Enhancers	Fetal Muscle Trunk	muscle
6	chr11:104797800-104798200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr11:104797800-104798200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
8	chr11:104798200-104798400	Flanking Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr11:104798200-104798400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr11:104798200-104798400	Enhancers	Primary T cells fromperipheralblood	blood
11	chr11:104798400-104798600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr11:104798400-104798600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr11:104803200-104803400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr11:104803400-104804000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr11:104803400-104819000	Weak transcription	Psoas Muscle	Psoas
16	chr11:104803600-104806200	Enhancers	Primary B cells from peripheral blood	blood
17	chr11:104804000-104805600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr11:104804200-104805400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
19	chr11:104804200-104806800	Enhancers	Primary T helper cells fromperipheralblood	blood
20	chr11:104804200-104806800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
21	chr11:104804200-104806800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr11:104804400-104805400	Enhancers	Primary B cells from cord blood	blood
23	chr11:104804600-104805200	Enhancers	Primary T helper cells PMA-I stimulated	--
24	chr11:104804600-104805400	Enhancers	Primary T cells from cord blood	blood
25	chr11:104804600-104805600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
26	chr11:104804600-104806200	Enhancers	Primary T cells fromperipheralblood	blood
27	chr11:104804600-104806200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
28	chr11:104804600-104806400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
29	chr11:104804600-104807000	Enhancers	Primary T killer memory cells from peripheral blood	blood
30	chr11:104805000-104805200	Enhancers	Primary T helper naive cells from peripheral blood	blood
31	chr11:104805000-104805200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:104805000-104806200	Enhancers	Dnd41	blood
33	chr11:104805000-104806800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr11:104805200-104805400	Enhancers	Spleen	Spleen
35	chr11:104805200-104805600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
36	chr11:104805200-104805600	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:104805200-104805600	Enhancers	Fetal Thymus	thymus
38	chr11:104805200-104805600	Enhancers	HUVEC	blood vessel
39	chr11:104805200-104805800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
40	chr11:104805200-104806000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr11:104805200-104806400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
42	chr11:104805200-104806600	Enhancers	Primary hematopoietic stem cells short term culture	blood
43	chr11:104805200-104806800	Enhancers	Primary hematopoietic stem cells	blood
44	chr11:104805400-104805600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:104805400-104805800	Flanking Active TSS	Primary T cells from cord blood	blood
46	chr11:104805400-104806000	Flanking Active TSS	Primary B cells from cord blood	blood
47	chr11:104805600-104805800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:104805600-104806000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
49	chr11:104805600-104807000	Enhancers	Primary T helper naive cells from peripheral blood	blood
50	chr11:104805600-104812600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood

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