Variant report

Variant	esv3450730
Chromosome Location	chr11:104938956-104968986
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	BATF	chr11:104948119-104948459	GM12878	blood:	n/a	chr11:104948321-104948332
2	CEBPB	chr11:104951117-104951358	IMR90	lung:	n/a	n/a
3	CEBPB	chr11:104948635-104948827	HepG2	liver:	n/a	chr11:104948658-104948669
4	CEBPB	chr11:104951169-104951316	Hela-S3	cervix:	n/a	n/a
5	CTCF	chr11:104943363-104943427	GM13976	blood:	n/a	n/a
6	CTCF	chr11:104945420-104945570	BE2_C	brain:	n/a	n/a
7	CTCF	chr11:104941845-104941925	Lung_OC	lung:	n/a	n/a
8	CTCF	chr11:104963580-104963730	HMEC	breast:	n/a	n/a
9	CTCF	chr11:104945394-104945576	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr11:104945360-104945510	AG09309	skin:	n/a	n/a
11	CTCF	chr11:104948711-104948822	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr11:104965975-104966006	GM20000	blood:	n/a	n/a
13	CTCF	chr11:104963760-104963910	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr11:104963680-104963830	HMEC	breast:	n/a	n/a
15	E2F4	chr11:104945873-104946021	MCF10A-Er-Src	breast:	n/a	n/a
16	EBF1	chr11:104946814-104946837	GM12878	blood:	n/a	chr11:104946815-104946826
17	FOS	chr11:104948262-104948729	MCF10A-Er-Src	breast:	n/a	n/a
18	FOS	chr11:104941207-104941399	MCF10A-Er-Src	breast:	n/a	chr11:104941311-104941321 chr11:104941311-104941321 chr11:104941308-104941319
19	FOS	chr11:104948211-104948907	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr11:104944266-104944785	HUVEC	blood vessel:	n/a	n/a
21	FOS	chr11:104941274-104941386	MCF10A-Er-Src	breast:	n/a	chr11:104941311-104941321 chr11:104941311-104941321 chr11:104941308-104941319
22	FOS	chr11:104942222-104942367	MCF10A-Er-Src	breast:	n/a	n/a
23	FOS	chr11:104963328-104963986	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
24	FOS	chr11:104948928-104949030	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr11:104963304-104963925	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
26	FOS	chr11:104941176-104941474	MCF10A-Er-Src	breast:	n/a	chr11:104941311-104941321 chr11:104941311-104941321 chr11:104941308-104941319
27	FOS	chr11:104963677-104964022	HUVEC	blood vessel:	n/a	chr11:104963836-104963847 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
28	FOS	chr11:104948241-104948837	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr11:104941168-104941469	MCF10A-Er-Src	breast:	n/a	chr11:104941311-104941321 chr11:104941311-104941321 chr11:104941308-104941319
30	FOS	chr11:104942242-104942452	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr11:104963304-104963982	MCF10A-Er-Src	breast:	n/a	chr11:104963836-104963847 chr11:104963362-104963369 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
32	FOS	chr11:104942187-104942387	MCF10A-Er-Src	breast:	n/a	n/a
33	FOXA2	chr11:104960656-104960851	HepG2	liver:	n/a	n/a
34	GATA2	chr11:104963362-104963700	SH-SY5Y	brain:	n/a	chr11:104963445-104963455
35	GATA3	chr11:104963287-104963717	SH-SY5Y	brain:	n/a	chr11:104963445-104963455
36	GATA3	chr11:104963367-104963635	MCF-7	breast:	n/a	chr11:104963445-104963455
37	JUN	chr11:104945011-104945062	K562	blood:	n/a	n/a
38	MAFF	chr11:104947432-104947580	HepG2	liver:	n/a	n/a
39	MAFF	chr11:104941396-104941578	HepG2	liver:	n/a	chr11:104941492-104941510
40	MAFK	chr11:104947352-104947628	HepG2	liver:	n/a	n/a
41	MAFK	chr11:104947451-104947500	HepG2	liver:	n/a	n/a
42	MAZ	chr11:104963309-104963476	HepG2	liver:	n/a	n/a
43	MYC	chr11:104940682-104940736	H1-hESC	embryonic stem cell:	n/a	n/a
44	MYC	chr11:104940722-104940734	HUVEC	blood vessel:	n/a	n/a
45	MYC	chr11:104940591-104940721	HUVEC	blood vessel:	n/a	n/a
46	MYC	chr11:104942084-104942475	MCF10A-Er-Src	breast:	n/a	n/a
47	MYC	chr11:104963215-104963761	MCF10A-Er-Src	breast:	n/a	n/a
48	MYC	chr11:104948687-104948837	MCF10A-Er-Src	breast:	n/a	n/a
49	MYC	chr11:104963252-104963831	MCF10A-Er-Src	breast:	n/a	n/a
50	MYC	chr11:104948580-104948902	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104966249-104966299	Caco-2	colon:	n/a
2	chr11:104966249-104966299	AG10803	skin:	n/a
3	chr11:104966249-104966299	HepG2	liver:	n/a
4	chr11:104966249-104966299	GM06990	blood:	n/a
5	chr11:104966249-104966299	AG09319	gingival:	n/a
6	chr11:104966249-104966299	PrEC	prostate:	n/a
7	chr11:104966249-104966299	HMEC	breast:	n/a
8	chr11:104966249-104966299	GM12891	blood:	n/a
9	chr11:104966249-104966299	ProgFib	skin:	n/a
10	chr11:104966249-104966299	ECC-1	luminal epithelium:	n/a
11	chr11:104966249-104966299	PANC-1	pancreas:	n/a
12	chr11:104966249-104966299	AoSMC	blood vessel:	n/a
13	chr11:104966249-104966299	Jurkat	blood:	n/a
14	chr11:104966249-104966299	SK-N-MC	brain:	n/a
15	chr11:104966249-104966299	MCF10A-Er-Src	breast:	n/a
16	chr11:104966249-104966299	HPAEpiC	pulmonary alveolar:	n/a
17	chr11:104966249-104966299	A549	lung:	n/a
18	chr11:104966249-104966299	U87	brain:	n/a
19	chr11:104966249-104966299	HCM	heart:	n/a
20	chr11:104966249-104966299	RPTEC	kidney:	n/a
21	chr11:104966249-104966299	HRPEpiC	eye:	n/a
22	chr11:104966249-104966299	NT2-D1	testis:	n/a
23	chr11:104966249-104966299	HL-60	blood:	n/a
24	chr11:104966249-104966299	K562	blood:	n/a
25	chr11:104966249-104966299	IMR90	lung:	fetal
26	chr11:104966249-104966299	BE2_C	brain:	n/a
27	chr11:104966249-104966299	HNPCEpiC	eye:	n/a
28	chr11:104966249-104966299	HAEpiC	amniotic membrane:	n/a
29	chr11:104966249-104966299	SK-N-SH	brain:	n/a
30	chr11:104966249-104966299	NH-A	brain:	n/a
31	chr11:104966249-104966299	HIPEpiC	eye:	n/a
32	chr11:104966249-104966299	HUVEC	blood vessel:	n/a
33	chr11:104966249-104966299	HEEpiC	esophagus:	n/a
34	chr11:104966249-104966299	SK-N-SH_RA	brain:	n/a
35	chr11:104966249-104966299	HCT-116	colon:	n/a
36	chr11:104966249-104966299	ovcar-3	ovarian:	n/a
37	chr11:104966249-104966299	HCF	heart:	n/a
38	chr11:104966249-104966299	H1-hESC	embryonic stem cell:	embryo
39	chr11:104966249-104966299	GM12878	blood:	n/a
40	chr11:104966249-104966299	Hepatocyte	liver:	n/a
41	chr11:104966249-104966299	AG04450	lung:	fetal
42	chr11:104966249-104966299	SKMC	muscle:	n/a
43	chr11:104966249-104966299	GM19239	blood:	n/a
44	chr11:104966249-104966299	HRCEpiC	kidney:	n/a
45	chr11:104966249-104966299	HRE	kidney:	n/a
46	chr11:104966249-104966299	HEK293	kidney:	embryo
47	chr11:104966249-104966299	SAEC	small airway:	n/a
48	chr11:104966249-104966299	Hela-S3	cervix:	n/a
49	chr11:104966249-104966299	BJ	skin:	n/a
50	chr11:104966249-104966299	AG04449	skin:	fetal

Variant related genes	Relation type
CASP1P2	TF binding region
CASP1P2	CpG island

Extended variants
information (count: 1124 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:1124 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs552100513	chr11:104938960-104938961	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144839117	chr11:104938975-104938976	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs537711090	chr11:104938977-104938978	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs72986774	chr11:104938979-104938980	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs567495951	chr11:104938988-104938989	Enhancers Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538943	chr11:104939029-104939030	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs538152	chr11:104939090-104939091	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs190766962	chr11:104939265-104939266	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs181611481	chr11:104939287-104939288	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs558851605	chr11:104939316-104939317	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs575458377	chr11:104939340-104939341	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs544447931	chr11:104939345-104939346	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs186894914	chr11:104939351-104939352	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs529900185	chr11:104939352-104939353	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs140338158	chr11:104939404-104939405	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs143730291	chr11:104939428-104939429	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs532175252	chr11:104939436-104939437	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs369652739	chr11:104939449-104939450	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs112780424	chr11:104939452-104939453	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs148109358	chr11:104939487-104939488	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs1630085	chr11:104939507-104939508	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs546384220	chr11:104939564-104939565	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs566469928	chr11:104939578-104939579	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs553460713	chr11:104939604-104939605	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373753583	chr11:104939647-104939648	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs551225230	chr11:104939659-104939660	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369341682	chr11:104939706-104939707	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs141854568	chr11:104939738-104939739	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs191776682	chr11:104939761-104939762	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1785869	chr11:104939776-104939777	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs2509634	chr11:104939840-104939841	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs539081341	chr11:104939858-104939859	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548205043	chr11:104939884-104939885	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs2511324	chr11:104939895-104939896	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs117327493	chr11:104939902-104939903	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs1212544	chr11:104939910-104939911	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs183179753	chr11:104939913-104939914	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs551058600	chr11:104939917-104939918	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs554882536	chr11:104939928-104939929	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs527704284	chr11:104939942-104939943	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs574733868	chr11:104939944-104939945	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs540420843	chr11:104939949-104939950	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs560350026	chr11:104939979-104939980	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138996871	chr11:104940048-104940049	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs377010082	chr11:104940060-104940061	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs78244300	chr11:104940082-104940083	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs186534346	chr11:104940102-104940103	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs189858677	chr11:104940156-104940157	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs570855860	chr11:104940168-104940169	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs540081812	chr11:104940172-104940173	Enhancers Weak transcription Flanking Active TSS Active TSS	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
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	18451855	CNVD

Chromatin state (count:233 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104935200-104941200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr11:104936200-104939000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
3	chr11:104936200-104939600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
4	chr11:104937600-104939800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
5	chr11:104938200-104941800	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr11:104938600-104939600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
7	chr11:104938600-104939600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
8	chr11:104938600-104939600	Weak transcription	Primary T helper cells fromperipheralblood	blood
9	chr11:104938800-104939400	Weak transcription	Primary T helper cells PMA-I stimulated	--
10	chr11:104939000-104940600	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
11	chr11:104939400-104940000	Enhancers	Primary T helper cells PMA-I stimulated	--
12	chr11:104939600-104939800	Enhancers	Primary T cells fromperipheralblood	blood
13	chr11:104939600-104940000	Enhancers	Primary T helper naive cells from peripheral blood	blood
14	chr11:104939600-104940200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
15	chr11:104939600-104940400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
16	chr11:104939600-104940400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
17	chr11:104939600-104941000	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
18	chr11:104939600-104941000	Enhancers	Primary T killer memory cells from peripheral blood	blood
19	chr11:104939800-104940200	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr11:104939800-104940400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
21	chr11:104939800-104940800	Weak transcription	NHEK	skin
22	chr11:104940000-104940200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
23	chr11:104940000-104940600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr11:104940000-104941000	Active TSS	Primary T helper naive cells from peripheral blood	blood
25	chr11:104940200-104940400	Flanking Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr11:104940200-104940800	Active TSS	Primary T helper cells PMA-I stimulated	--
27	chr11:104940200-104941400	Enhancers	Monocytes-CD14+_RO01746	blood
28	chr11:104940200-104942400	Active TSS	Primary T cells fromperipheralblood	blood
29	chr11:104940400-104940800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
30	chr11:104940400-104940800	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr11:104940400-104941000	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
32	chr11:104940400-104941000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
33	chr11:104940600-104941000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr11:104940600-104941400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
35	chr11:104940600-104941400	Enhancers	Dnd41	blood
36	chr11:104940800-104941000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
37	chr11:104940800-104941200	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
38	chr11:104940800-104941400	Enhancers	NHEK	skin
39	chr11:104940800-104941600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
40	chr11:104940800-104943200	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr11:104941000-104941200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
42	chr11:104941000-104941400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
43	chr11:104941000-104941400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr11:104941000-104941400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
45	chr11:104941000-104941600	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
46	chr11:104941000-104941800	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chr11:104941000-104942000	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
48	chr11:104941000-104942200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr11:104941000-104942600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr11:104941000-104942600	Enhancers	Primary neutrophils fromperipheralblood	blood

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