Variant report

Variant	nsv524985
Chromosome Location	chr11:104960997-104991640
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	chr11:104978298-104978484	GM12878	blood:	n/a	chr11:104978391-104978402
2	BATF	chr11:104970890-104971077	GM12878	blood:	n/a	n/a
3	BRCA1	chr11:104981132-104981302	Hela-S3	cervix:	n/a	n/a
4	BRCA1	chr11:104980114-104980416	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr11:104981081-104981355	IMR90	lung:	n/a	n/a
6	CEBPB	chr11:104978090-104978147	HepG2	liver:	n/a	chr11:104978093-104978104
7	CEBPB	chr11:104978051-104978186	Hela-S3	cervix:	n/a	chr11:104978093-104978104
8	CEBPB	chr11:104983146-104983401	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr11:104980621-104981623	Hela-S3	cervix:	n/a	chr11:104981527-104981539
10	CEBPB	chr11:104978050-104978162	IMR90	lung:	n/a	chr11:104978093-104978104
11	CEBPB	chr11:104979651-104980417	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr11:104980755-104981370	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr11:104963760-104963910	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr11:104963580-104963730	HMEC	breast:	n/a	n/a
15	CTCF	chr11:104963680-104963830	HMEC	breast:	n/a	n/a
16	CTCF	chr11:104987320-104987470	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr11:104991553-104991614	GM13976	blood:	n/a	n/a
18	CTCF	chr11:104971768-104971837	GM10266	blood:	n/a	n/a
19	CTCF	chr11:104979306-104979337	Lung_OC	lung:	n/a	n/a
20	CTCF	chr11:104972751-104972831	Spleen_OC	spleen:	n/a	n/a
21	CTCF	chr11:104965975-104966006	GM20000	blood:	n/a	n/a
22	E2F4	chr11:104984402-104984512	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr11:104985599-104985639	MCF10A-Er-Src	breast:	n/a	n/a
24	EP300	chr11:104980066-104980404	Hela-S3	cervix:	n/a	n/a
25	EP300	chr11:104980674-104981354	Hela-S3	cervix:	n/a	chr11:104981322-104981336 chr11:104981324-104981338 chr11:104981328-104981342 chr11:104981052-104981062
26	FOS	chr11:104984339-104984638	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr11:104984332-104984659	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr11:104972012-104972419	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr11:104984366-104984632	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr11:104972042-104972303	MCF10A-Er-Src	breast:	n/a	n/a
31	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
32	FOS	chr11:104970870-104971415	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
33	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
34	FOS	chr11:104963677-104964022	HUVEC	blood vessel:	n/a	chr11:104963836-104963847 chr11:104963838-104963845 chr11:104963838-104963846 chr11:104963838-104963847 chr11:104963837-104963846
35	FOS	chr11:104970925-104971329	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
36	FOS	chr11:104981163-104981300	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr11:104970874-104971326	HUVEC	blood vessel:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
38	FOS	chr11:104980229-104980300	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr11:104971878-104972346	MCF10A-Er-Src	breast:	n/a	chr11:104971936-104971945
40	FOS	chr11:104971940-104972376	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr11:104981126-104981606	HUVEC	blood vessel:	n/a	n/a
42	FOS	chr11:104970836-104971491	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
43	FOS	chr11:104970835-104971425	MCF10A-Er-Src	breast:	n/a	chr11:104971220-104971230 chr11:104971217-104971228 chr11:104971220-104971230 chr11:104971221-104971230
44	FOS	chr11:104980126-104980399	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr11:104980111-104980404	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr11:104980051-104980413	MCF10A-Er-Src	breast:	n/a	n/a
47	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
48	FOS	chr11:104984337-104984625	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr11:104981257-104981290	MCF10A-Er-Src	breast:	n/a	n/a
50	FOXA1	chr11:104980838-104981137	T-47D	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104966249-104966299	IMR90	lung:	fetal
2	chr11:104966249-104966299	HCPEpiC	choroid plexus:	n/a
3	chr11:104966249-104966299	IMR90	lung:	fetal
4	chr11:104966249-104966299	HCPEpiC	choroid plexus:	n/a
5	chr11:104966249-104966299	A549	lung:	n/a
6	chr11:104966249-104966299	HIPEpiC	eye:	n/a
7	chr11:104972135-104972185	ovcar-3	ovarian:	n/a
8	chr11:104972078-104972128	H1-hESC	embryonic stem cell:	embryo
9	chr11:104972078-104972128	AG10803	skin:	n/a
10	chr11:104966249-104966299	Hepatocyte	liver:	n/a
11	chr11:104972135-104972185	PrEC	prostate:	n/a
12	chr11:104972078-104972128	SKMC	muscle:	n/a
13	chr11:104972135-104972185	HL-60	blood:	n/a
14	chr11:104972078-104972128	HCPEpiC	choroid plexus:	n/a
15	chr11:104972907-104972957	RPTEC	kidney:	n/a
16	chr11:104973640-104973690	AoSMC	blood vessel:	n/a
17	chr11:104966249-104966299	AG04449	skin:	fetal
18	chr11:104972907-104972957	AG09319	gingival:	n/a
19	chr11:104972078-104972128	HEEpiC	esophagus:	n/a
20	chr11:104972907-104972957	HMEC	breast:	n/a
21	chr11:104972078-104972128	NT2-D1	testis:	n/a
22	chr11:104966249-104966299	ECC-1	luminal epithelium:	n/a
23	chr11:104972907-104972957	SAEC	small airway:	n/a
24	chr11:104973640-104973690	NH-A	brain:	n/a
25	chr11:104973640-104973690	MCF-7	breast:	n/a
26	chr11:104966249-104966299	HL-60	blood:	n/a
27	chr11:104973640-104973690	NT2-D1	testis:	n/a
28	chr11:104972907-104972957	GM06990	blood:	n/a
29	chr11:104973640-104973690	HMEC	breast:	n/a
30	chr11:104972078-104972128	Hepatocyte	liver:	n/a
31	chr11:104972474-104972524	U87	brain:	n/a
32	chr11:104966249-104966299	GM12878	blood:	n/a
33	chr11:104972135-104972185	AG09309	skin:	n/a
34	chr11:104972474-104972524	IMR90	lung:	fetal
35	chr11:104972474-104972524	PANC-1	pancreas:	n/a
36	chr11:104972078-104972128	HPAEpiC	pulmonary alveolar:	n/a
37	chr11:104972135-104972185	LNCaP	prostate:	n/a
38	chr11:104972474-104972524	NHBE	bronchial:	n/a
39	chr11:104972474-104972524	CMK	blood:	n/a
40	chr11:104972078-104972128	K562	blood:	n/a
41	chr11:104972135-104972185	GM06990	blood:	n/a
42	chr11:104972474-104972524	HL-60	blood:	n/a
43	chr11:104972078-104972128	SK-N-SH	brain:	n/a
44	chr11:104972078-104972128	SK-N-SH_RA	brain:	n/a
45	chr11:104966249-104966299	AoSMC	blood vessel:	n/a
46	chr11:104972474-104972524	ECC-1	luminal epithelium:	n/a
47	chr11:104973640-104973690	Hela-S3	cervix:	n/a
48	chr11:104972135-104972185	U87	brain:	n/a
49	chr11:104973640-104973690	BJ	skin:	n/a
50	chr11:104972135-104972185	Hela-S3	cervix:	n/a

Variant related genes	Relation type
CASP1	TF binding region
CARD16	TF binding region
CARD17	TF binding region
CASP1	CpG island
CARD16	CpG island
CARD17	CpG island

Extended variants
information (count: 1000 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:1000 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575792143	chr11:104961820-104961821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529379279	chr11:104961833-104961834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs370690989	chr11:104961838-104961839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370296586	chr11:104961855-104961856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113147365	chr11:104961896-104961897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs184160669	chr11:104961929-104961930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs540655212	chr11:104961976-104961977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs145820002	chr11:104961991-104961992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374750995	chr11:104962002-104962003	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1792764	chr11:104962019-104962020	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs148969436	chr11:104962020-104962021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs552047303	chr11:104962063-104962064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567091753	chr11:104962086-104962087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571064836	chr11:104962122-104962123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531410214	chr11:104962129-104962130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547932662	chr11:104962131-104962132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561467645	chr11:104962197-104962198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112706051	chr11:104962229-104962230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547110890	chr11:104962318-104962319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370670854	chr11:104962320-104962321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115343459	chr11:104962327-104962328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs111489217	chr11:104962346-104962347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs187788242	chr11:104962390-104962391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116836533	chr11:104962399-104962400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs538446552	chr11:104962438-104962439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555175260	chr11:104962470-104962471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs138272830	chr11:104962557-104962558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575003843	chr11:104962564-104962565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs199918268	chr11:104962592-104962593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376807827	chr11:104962593-104962594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200982238	chr11:104962594-104962595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs372237957	chr11:104962595-104962596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539991463	chr11:104962597-104962598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs377242278	chr11:104962645-104962646	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs577156690	chr11:104962670-104962671	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs147793122	chr11:104962783-104962784	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs562803384	chr11:104962790-104962791	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555848136	chr11:104962807-104962808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553748002	chr11:104962862-104962863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs541645691	chr11:104962866-104962867	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs561524618	chr11:104962897-104962898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2019290	chr11:104962900-104962901	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1960620	chr11:104962984-104962985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs117930590	chr11:104963033-104963034	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs538498992	chr11:104963041-104963042	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs193136872	chr11:104963095-104963096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs563972636	chr11:104963098-104963099	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs141154072	chr11:104963102-104963103	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs1785878	chr11:104963106-104963107	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs549469664	chr11:104963108-104963109	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104961800-104962000	Enhancers	Breast Myoepithelial Primary Cells	Breast
2	chr11:104962000-104962800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr11:104962600-104963600	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr11:104962800-104963000	Enhancers	Breast Myoepithelial Primary Cells	Breast
5	chr11:104962800-104963600	Enhancers	Monocytes-CD14+_RO01746	blood
6	chr11:104962800-104964000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr11:104962800-104964400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
8	chr11:104963000-104963200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr11:104963000-104963200	Enhancers	NHEK	skin
10	chr11:104963000-104963400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr11:104963000-104963400	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr11:104963000-104963400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr11:104963000-104964400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr11:104963200-104963400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr11:104963200-104963400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr11:104963200-104963400	Active TSS	HMEC	breast
17	chr11:104963200-104964000	Enhancers	Hela-S3	cervix
18	chr11:104963200-104964200	Flanking Active TSS	NHEK	skin
19	chr11:104963400-104963600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr11:104963400-104963800	Active TSS	Breast Myoepithelial Primary Cells	Breast
21	chr11:104963400-104963800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr11:104963400-104963800	Flanking Active TSS	HMEC	breast
23	chr11:104963400-104970200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
24	chr11:104963600-104963800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr11:104963800-104964200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr11:104963800-104964200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr11:104963800-104964200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr11:104963800-104964200	Enhancers	HMEC	breast
29	chr11:104964200-104964400	Enhancers	Breast Myoepithelial Primary Cells	Breast
30	chr11:104964200-104964400	Enhancers	NHEK	skin
31	chr11:104964400-104969600	Weak transcription	NHEK	skin
32	chr11:104964400-104971600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr11:104966200-104969600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
34	chr11:104968000-104969600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
35	chr11:104968600-104970000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
36	chr11:104969600-104970200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
37	chr11:104969600-104970200	Enhancers	Primary T helper cells PMA-I stimulated	--
38	chr11:104969600-104970200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr11:104969600-104970600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
40	chr11:104969600-104970600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
41	chr11:104969600-104972200	Enhancers	NHEK	skin
42	chr11:104969800-104970800	Enhancers	Primary T helper naive cells from peripheral blood	blood
43	chr11:104970000-104970200	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chr11:104970000-104970400	Enhancers	Monocytes-CD14+_RO01746	blood
45	chr11:104970000-104970800	Enhancers	Primary neutrophils fromperipheralblood	blood
46	chr11:104970000-104971000	Enhancers	Primary T helper cells fromperipheralblood	blood
47	chr11:104970000-104974200	Enhancers	Primary monocytes fromperipheralblood	blood
48	chr11:104970200-104970400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
49	chr11:104970200-104970600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr11:104970200-104970800	Active TSS	Primary T helper 17 cells PMA-I stimulated	--

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