Variant report

Variant	esv3356969
Chromosome Location	chr11:104786594-104803934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:37)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:37 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr11:104789758-104789850	A549	lung:	n/a	n/a
2	CHD2	chr11:104796787-104796814	HepG2	liver:	n/a	n/a
3	CTCF	chr11:104789807-104789835	Lung_OC	lung:	n/a	n/a
4	CTCF	chr11:104797580-104797730	GM12864	blood:	n/a	n/a
5	CTCF	chr11:104797685-104797749	H1-hESC	embryonic stem cell:	n/a	n/a
6	E2F4	chr11:104788905-104789105	MCF10A-Er-Src	breast:	n/a	n/a
7	FOS	chr11:104788862-104789127	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr11:104788795-104789127	MCF10A-Er-Src	breast:	n/a	n/a
9	FOXA1	chr11:104796527-104796907	HepG2	liver:	n/a	n/a
10	FOXA1	chr11:104796560-104796871	HepG2	liver:	n/a	n/a
11	FOXA1	chr11:104796521-104797007	HepG2	liver:	n/a	n/a
12	FOXA1	chr11:104796564-104796856	HepG2	liver:	n/a	n/a
13	FOXA2	chr11:104796607-104796854	HepG2	liver:	n/a	n/a
14	JUN	chr11:104788768-104789194	HUVEC	blood vessel:	n/a	n/a
15	MAFK	chr11:104788919-104789093	HepG2	liver:	n/a	chr11:104789005-104789021
16	MAFK	chr11:104798723-104798922	HepG2	liver:	n/a	n/a
17	MAFK	chr11:104788844-104789179	IMR90	lung:	n/a	chr11:104789005-104789021
18	MAZ	chr11:104797800-104798232	IMR90	lung:	n/a	n/a
19	MAZ	chr11:104797857-104797931	HepG2	liver:	n/a	n/a
20	POLR2A	chr11:104788488-104789400	HUVEC	blood vessel:	n/a	n/a
21	POLR2A	chr11:104785665-104789803	HUVEC	blood vessel:	n/a	n/a
22	POLR2A	chr11:104790225-104790374	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr11:104788729-104789148	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr11:104800704-104800828	MCF10A-Er-Src	breast:	n/a	n/a
25	POLR2A	chr11:104788835-104789113	MCF10A-Er-Src	breast:	n/a	n/a
26	SPI1	chr11:104792741-104792961	GM12891	blood:	n/a	n/a
27	SPI1	chr11:104792803-104792893	GM12878	blood:	n/a	n/a
28	STAT3	chr11:104788832-104789060	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944 chr11:104788897-104788908
29	STAT3	chr11:104787317-104787328	MCF10A-Er-Src	breast:	n/a	n/a
30	STAT3	chr11:104788763-104789072	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944 chr11:104788897-104788908
31	STAT3	chr11:104788936-104789039	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944
32	STAT3	chr11:104789542-104789554	MCF10A-Er-Src	breast:	n/a	n/a
33	STAT3	chr11:104788686-104788849	MCF10A-Er-Src	breast:	n/a	n/a
34	TCF12	chr11:104797812-104798108	H1-hESC	embryonic stem cell:	n/a	n/a
35	TEAD4	chr11:104797824-104798213	H1-hESC	embryonic stem cell:	n/a	n/a
36	TEAD4	chr11:104797800-104798092	H1-hESC	embryonic stem cell:	n/a	n/a
37	YY1	chr11:104796513-104797031	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104789337-104789387	HEK293	kidney:	embryo
2	chr11:104789052-104789102	GM12891	blood:	n/a
3	chr11:104789052-104789102	HCF	heart:	n/a
4	chr11:104789337-104789387	HepG2	liver:	n/a
5	chr11:104789052-104789102	MCF-7	breast:	n/a
6	chr11:104789337-104789387	LNCaP	prostate:	n/a
7	chr11:104789337-104789387	GM12892	blood:	n/a
8	chr11:104789337-104789387	GM12891	blood:	n/a
9	chr11:104789052-104789102	GM12878	blood:	n/a
10	chr11:104789337-104789387	NT2-D1	testis:	n/a
11	chr11:104789052-104789102	HAEpiC	amniotic membrane:	n/a
12	chr11:104789052-104789102	SKMC	muscle:	n/a
13	chr11:104789337-104789387	SKMC	muscle:	n/a
14	chr11:104789337-104789387	Hepatocyte	liver:	n/a
15	chr11:104789337-104789387	PANC-1	pancreas:	n/a
16	chr11:104789337-104789387	HCPEpiC	choroid plexus:	n/a
17	chr11:104789052-104789102	HNPCEpiC	eye:	n/a
18	chr11:104789052-104789102	AoSMC	blood vessel:	n/a
19	chr11:104789052-104789102	HRCEpiC	kidney:	n/a
20	chr11:104789052-104789102	GM12892	blood:	n/a
21	chr11:104789337-104789387	GM19239	blood:	n/a
22	chr11:104789337-104789387	AG09309	skin:	n/a
23	chr11:104789052-104789102	NHDF-neo	bronchial:	n/a
24	chr11:104789052-104789102	ECC-1	luminal epithelium:	n/a
25	chr11:104789337-104789387	U87	brain:	n/a
26	chr11:104789337-104789387	AoSMC	blood vessel:	n/a
27	chr11:104789052-104789102	SK-N-MC	brain:	n/a
28	chr11:104789337-104789387	ECC-1	luminal epithelium:	n/a
29	chr11:104789337-104789387	NHBE	bronchial:	n/a
30	chr11:104789052-104789102	Hepatocyte	liver:	n/a
31	chr11:104789052-104789102	HPAEpiC	pulmonary alveolar:	n/a
32	chr11:104789337-104789387	ovcar-3	ovarian:	n/a
33	chr11:104789052-104789102	HCPEpiC	choroid plexus:	n/a
34	chr11:104789337-104789387	AG09319	gingival:	n/a
35	chr11:104789337-104789387	A549	lung:	n/a
36	chr11:104789337-104789387	BE2_C	brain:	n/a
37	chr11:104789052-104789102	NH-A	brain:	n/a
38	chr11:104789052-104789102	HL-60	blood:	n/a
39	chr11:104789052-104789102	GM19239	blood:	n/a
40	chr11:104789337-104789387	Jurkat	blood:	n/a
41	chr11:104789337-104789387	SK-N-MC	brain:	n/a
42	chr11:104789052-104789102	NT2-D1	testis:	n/a
43	chr11:104789337-104789387	HL-60	blood:	n/a
44	chr11:104789052-104789102	LNCaP	prostate:	n/a
45	chr11:104789337-104789387	AG04449	skin:	fetal
46	chr11:104789337-104789387	HAEpiC	amniotic membrane:	n/a
47	chr11:104789337-104789387	K562	blood:	n/a
48	chr11:104789052-104789102	HUVEC	blood vessel:	n/a
49	chr11:104789052-104789102	ovcar-3	ovarian:	n/a
50	chr11:104789052-104789102	PANC-1	pancreas:	n/a

No data

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CASP12-3	chr11:104789658-104789800	NONHSAT023943
2	lnc-CASP12-3	chr11:104788840-104788902	NR_034079
3	lnc-CASP12-3	chr11:104788840-104788902	NR_034078
4	lnc-CASP12-3	chr11:104788840-104788870	NONHSAT023944

No data

Variant related genes	Relation type
ENSG00000235505	TF binding region
ENSG00000235505	CpG island

Extended variants
information (count: 371 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:371 , 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	rs371494151	chr11:104786609-104786610	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs557487729	chr11:104786619-104786620	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs12417315	chr11:104786630-104786631	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs536609736	chr11:104786632-104786633	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs577156932	chr11:104786652-104786653	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs9326348	chr11:104786653-104786654	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs2851168	chr11:104786729-104786730	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs558749560	chr11:104786731-104786732	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs548810699	chr11:104786797-104786798	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs543946299	chr11:104786839-104786840	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs675358	chr11:104786856-104786857	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs78939703	chr11:104786860-104786861	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs368562011	chr11:104786906-104786907	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs551312	chr11:104786973-104786974	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs191639977	chr11:104787060-104787061	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs567440654	chr11:104787081-104787082	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs551781091	chr11:104787153-104787154	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs571860066	chr11:104787159-104787160	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs531081048	chr11:104787227-104787228	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs115917354	chr11:104787233-104787234	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs567730023	chr11:104787262-104787263	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs138346813	chr11:104787340-104787341	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs553359610	chr11:104787354-104787355	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs77553750	chr11:104787407-104787408	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs200007963	chr11:104787421-104787422	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs535594081	chr11:104787442-104787443	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs182306308	chr11:104787480-104787481	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs530712233	chr11:104787530-104787531	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77559258	chr11:104787532-104787533	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs572712495	chr11:104787559-104787560	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12294079	chr11:104787564-104787565	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs10466555	chr11:104787578-104787579	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs187502392	chr11:104787624-104787625	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs554257708	chr11:104787632-104787633	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs71471748	chr11:104787662-104787663	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs10466650	chr11:104787664-104787665	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs560134834	chr11:104787668-104787669	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs532008401	chr11:104787675-104787676	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs545689801	chr11:104787689-104787690	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs111959719	chr11:104787759-104787760	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs531146626	chr11:104787869-104787870	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551168808	chr11:104787871-104787872	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs201144823	chr11:104787878-104787879	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs72116027	chr11:104787879-104787880	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200921897	chr11:104787884-104787885	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs113734694	chr11:104787902-104787903	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs530249906	chr11:104787906-104787907	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs546767257	chr11:104787936-104787937	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs550829445	chr11:104787938-104787939	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs193267279	chr11:104787988-104787989	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
Tetralogy of Fallot	22912587	CNVD
Prostate cancer	18632612	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:297 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104769200-104786600	Weak transcription	Fetal Muscle Leg	muscle
2	chr11:104769200-104787800	Weak transcription	Fetal Lung	lung
3	chr11:104769400-104786800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr11:104769600-104786800	Weak transcription	Adipose Nuclei	Adipose
5	chr11:104769600-104788000	Weak transcription	Fetal Stomach	stomach
6	chr11:104770400-104786600	Weak transcription	Ovary	ovary
7	chr11:104776400-104787200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr11:104778400-104786800	Weak transcription	Aorta	Aorta
9	chr11:104778400-104788800	Weak transcription	Pancreas	Pancrea
10	chr11:104779000-104786800	Weak transcription	NHLF	lung
11	chr11:104779200-104788000	Weak transcription	Fetal Muscle Trunk	muscle
12	chr11:104779800-104786600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
13	chr11:104779800-104786600	Weak transcription	Left Ventricle	heart
14	chr11:104782200-104786600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr11:104783400-104786800	Weak transcription	Dnd41	blood
16	chr11:104783600-104786600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr11:104783800-104788000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
18	chr11:104784400-104787000	Enhancers	Primary T helper cells fromperipheralblood	blood
19	chr11:104784600-104786600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
20	chr11:104785200-104786600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr11:104785200-104787200	Enhancers	Breast Myoepithelial Primary Cells	Breast
22	chr11:104785400-104786600	Weak transcription	Small Intestine	intestine
23	chr11:104785400-104786800	Enhancers	Primary T killer memory cells from peripheral blood	blood
24	chr11:104785400-104787000	Enhancers	Psoas Muscle	Psoas
25	chr11:104785600-104786800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
26	chr11:104785600-104787000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
27	chr11:104785600-104788000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr11:104785800-104787200	Weak transcription	Rectal Smooth Muscle	rectum
29	chr11:104786000-104786800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
30	chr11:104786000-104787000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr11:104786000-104788000	Enhancers	Primary B cells from peripheral blood	blood
32	chr11:104786400-104786600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr11:104786400-104786600	Active TSS	Primary T cells fromperipheralblood	blood
34	chr11:104786400-104787000	Enhancers	Skeletal Muscle Female	skeletal muscle
35	chr11:104786600-104786800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr11:104786600-104786800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
37	chr11:104786600-104786800	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
38	chr11:104786600-104786800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr11:104786600-104786800	Enhancers	Lung	lung
40	chr11:104786600-104786800	Enhancers	Right Atrium	heart
41	chr11:104786600-104786800	Enhancers	HUVEC	blood vessel
42	chr11:104786600-104787000	Flanking Active TSS	Primary T cells fromperipheralblood	blood
43	chr11:104786600-104787000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
44	chr11:104786600-104787000	Enhancers	Fetal Muscle Leg	muscle
45	chr11:104786600-104787000	Enhancers	Left Ventricle	heart
46	chr11:104786600-104787000	Enhancers	Sigmoid Colon	Sigmoid Colon
47	chr11:104786600-104787000	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr11:104786600-104787000	Enhancers	Small Intestine	intestine
49	chr11:104786600-104787200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr11:104786600-104787200	Enhancers	Ovary	ovary

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