Variant report

Variant	nsv983232
Chromosome Location	chr11:104787454-104809055
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:44)
CpG islands
(count:122)
Chromatin interactive
region (count:0)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:44 , 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	chr11:104797580-104797730	GM12864	blood:	n/a	n/a
4	CTCF	chr11:104789807-104789835	Lung_OC	lung:	n/a	n/a
5	CTCF	chr11:104797685-104797749	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr11:104805280-104805430	GM12874	blood:	n/a	n/a
7	E2F4	chr11:104788905-104789105	MCF10A-Er-Src	breast:	n/a	n/a
8	FOS	chr11:104788862-104789127	MCF10A-Er-Src	breast:	n/a	n/a
9	FOS	chr11:104788795-104789127	MCF10A-Er-Src	breast:	n/a	n/a
10	FOXA1	chr11:104796521-104797007	HepG2	liver:	n/a	n/a
11	FOXA1	chr11:104796527-104796907	HepG2	liver:	n/a	n/a
12	FOXA1	chr11:104796564-104796856	HepG2	liver:	n/a	n/a
13	FOXA1	chr11:104796560-104796871	HepG2	liver:	n/a	n/a
14	FOXA2	chr11:104796607-104796854	HepG2	liver:	n/a	n/a
15	JUN	chr11:104788768-104789194	HUVEC	blood vessel:	n/a	n/a
16	MAFK	chr11:104788919-104789093	HepG2	liver:	n/a	chr11:104789005-104789021
17	MAFK	chr11:104798723-104798922	HepG2	liver:	n/a	n/a
18	MAFK	chr11:104788844-104789179	IMR90	lung:	n/a	chr11:104789005-104789021
19	MAZ	chr11:104797857-104797931	HepG2	liver:	n/a	n/a
20	MAZ	chr11:104797800-104798232	IMR90	lung:	n/a	n/a
21	MEF2A	chr11:104805358-104805737	GM12878	blood:	n/a	n/a
22	MYC	chr11:104808166-104808332	MCF10A-Er-Src	breast:	n/a	n/a
23	POLR2A	chr11:104808596-104808776	MCF10A-Er-Src	breast:	n/a	n/a
24	POLR2A	chr11:104785665-104789803	HUVEC	blood vessel:	n/a	n/a
25	POLR2A	chr11:104806637-104806763	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr11:104790225-104790374	MCF10A-Er-Src	breast:	n/a	n/a
27	POLR2A	chr11:104788835-104789113	MCF10A-Er-Src	breast:	n/a	n/a
28	POLR2A	chr11:104788488-104789400	HUVEC	blood vessel:	n/a	n/a
29	POLR2A	chr11:104800704-104800828	MCF10A-Er-Src	breast:	n/a	n/a
30	POLR2A	chr11:104808694-104808704	MCF10A-Er-Src	breast:	n/a	n/a
31	POLR2A	chr11:104806810-104806882	MCF10A-Er-Src	breast:	n/a	n/a
32	POLR2A	chr11:104788729-104789148	MCF10A-Er-Src	breast:	n/a	n/a
33	SPI1	chr11:104792741-104792961	GM12891	blood:	n/a	n/a
34	SPI1	chr11:104792803-104792893	GM12878	blood:	n/a	n/a
35	STAT3	chr11:104788763-104789072	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944 chr11:104788897-104788908
36	STAT3	chr11:104788936-104789039	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944
37	STAT3	chr11:104788832-104789060	MCF10A-Er-Src	breast:	n/a	chr11:104788998-104789006 chr11:104788937-104788944 chr11:104788897-104788908
38	STAT3	chr11:104788686-104788849	MCF10A-Er-Src	breast:	n/a	n/a
39	STAT3	chr11:104789542-104789554	MCF10A-Er-Src	breast:	n/a	n/a
40	TCF12	chr11:104797812-104798108	H1-hESC	embryonic stem cell:	n/a	n/a
41	TEAD4	chr11:104797800-104798092	H1-hESC	embryonic stem cell:	n/a	n/a
42	TEAD4	chr11:104797824-104798213	H1-hESC	embryonic stem cell:	n/a	n/a
43	YY1	chr11:104796513-104797031	HepG2	liver:	n/a	n/a
44	ZNF384	chr11:104805522-104805561	GM12878	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr11:104789052-104789102	RPTEC	kidney:	n/a
2	chr11:104789337-104789387	U87	brain:	n/a
3	chr11:104789337-104789387	BE2_C	brain:	n/a
4	chr11:104789052-104789102	Caco-2	colon:	n/a
5	chr11:104789052-104789102	AG10803	skin:	n/a
6	chr11:104789337-104789387	GM12892	blood:	n/a
7	chr11:104789052-104789102	HCPEpiC	choroid plexus:	n/a
8	chr11:104789337-104789387	LNCaP	prostate:	n/a
9	chr11:104789337-104789387	HEK293	kidney:	embryo
10	chr11:104789337-104789387	HL-60	blood:	n/a
11	chr11:104789052-104789102	K562	blood:	n/a
12	chr11:104789337-104789387	SK-N-MC	brain:	n/a
13	chr11:104789052-104789102	GM12891	blood:	n/a
14	chr11:104789337-104789387	A549	lung:	n/a
15	chr11:104789052-104789102	HRE	kidney:	n/a
16	chr11:104789337-104789387	PrEC	prostate:	n/a
17	chr11:104789052-104789102	GM12892	blood:	n/a
18	chr11:104789052-104789102	Jurkat	blood:	n/a
19	chr11:104789052-104789102	AG09319	gingival:	n/a
20	chr11:104789337-104789387	SKMC	muscle:	n/a
21	chr11:104789337-104789387	HMEC	breast:	n/a
22	chr11:104789052-104789102	AG04450	lung:	fetal
23	chr11:104789052-104789102	BJ	skin:	n/a
24	chr11:104789337-104789387	HCT-116	colon:	n/a
25	chr11:104789337-104789387	GM19239	blood:	n/a
26	chr11:104789337-104789387	T-47D	breast:	n/a
27	chr11:104789337-104789387	HNPCEpiC	eye:	n/a
28	chr11:104789052-104789102	PrEC	prostate:	n/a
29	chr11:104789052-104789102	HRPEpiC	eye:	n/a
30	chr11:104789052-104789102	HNPCEpiC	eye:	n/a
31	chr11:104789052-104789102	MCF10A-Er-Src	breast:	n/a
32	chr11:104789052-104789102	NHBE	bronchial:	n/a
33	chr11:104789337-104789387	HCPEpiC	choroid plexus:	n/a
34	chr11:104789337-104789387	NT2-D1	testis:	n/a
35	chr11:104789337-104789387	ProgFib	skin:	n/a
36	chr11:104789052-104789102	MCF-7	breast:	n/a
37	chr11:104789052-104789102	SK-N-MC	brain:	n/a
38	chr11:104789337-104789387	GM12891	blood:	n/a
39	chr11:104789052-104789102	HRCEpiC	kidney:	n/a
40	chr11:104789337-104789387	Hela-S3	cervix:	n/a
41	chr11:104789337-104789387	HRE	kidney:	n/a
42	chr11:104789052-104789102	T-47D	breast:	n/a
43	chr11:104789052-104789102	PANC-1	pancreas:	n/a
44	chr11:104789337-104789387	IMR90	lung:	fetal
45	chr11:104789052-104789102	Hela-S3	cervix:	n/a
46	chr11:104789337-104789387	SK-N-SH_RA	brain:	n/a
47	chr11:104789337-104789387	AoSMC	blood vessel:	n/a
48	chr11:104789052-104789102	U87	brain:	n/a
49	chr11:104789337-104789387	ovcar-3	ovarian:	n/a
50	chr11:104789337-104789387	AG09319	gingival:	n/a

No data

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

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

No data

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

Extended variants
information (count: 554 )
Associated
traits (count: 93 )

Variant overlapped rSNPs/rCNVs (count:554 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182306308	chr11:104787480-104787481	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs530712233	chr11:104787530-104787531	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs77559258	chr11:104787532-104787533	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs572712495	chr11:104787559-104787560	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs12294079	chr11:104787564-104787565	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs10466555	chr11:104787578-104787579	Enhancers Weak transcription Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs187502392	chr11:104787624-104787625	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs554257708	chr11:104787632-104787633	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs71471748	chr11:104787662-104787663	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs10466650	chr11:104787664-104787665	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs560134834	chr11:104787668-104787669	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs532008401	chr11:104787675-104787676	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs545689801	chr11:104787689-104787690	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs111959719	chr11:104787759-104787760	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs531146626	chr11:104787869-104787870	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs551168808	chr11:104787871-104787872	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs201144823	chr11:104787878-104787879	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs72116027	chr11:104787879-104787880	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs200921897	chr11:104787884-104787885	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs113734694	chr11:104787902-104787903	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs530249906	chr11:104787906-104787907	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs546767257	chr11:104787936-104787937	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs550829445	chr11:104787938-104787939	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs193267279	chr11:104787988-104787989	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs538609264	chr11:104788001-104788002	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs147242300	chr11:104788013-104788014	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs520173	chr11:104788061-104788062	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
28	rs537670486	chr11:104788099-104788100	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs75246162	chr11:104788134-104788135	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs574283935	chr11:104788135-104788136	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs533936039	chr11:104788148-104788149	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs555122234	chr11:104788199-104788200	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs12282244	chr11:104788252-104788253	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs648421	chr11:104788304-104788305	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs185678225	chr11:104788313-104788314	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs518128	chr11:104788337-104788338	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs75145264	chr11:104788338-104788339	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs78401313	chr11:104788353-104788354	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs558934056	chr11:104788354-104788355	Weak transcription Flanking Active TSS Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs76389443	chr11:104788456-104788457	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs547070644	chr11:104788474-104788475	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs373156263	chr11:104788517-104788518	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs532553560	chr11:104788572-104788573	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs552259322	chr11:104788579-104788580	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141563732	chr11:104788588-104788589	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs537790067	chr11:104788607-104788608	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs577421613	chr11:104788636-104788637	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs567917790	chr11:104788693-104788694	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs533710882	chr11:104788694-104788695	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs514537	chr11:104788727-104788728	Active TSS Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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

Chromatin state (count:309 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:104769200-104787800	Weak transcription	Fetal Lung	lung
2	chr11:104769600-104788000	Weak transcription	Fetal Stomach	stomach
3	chr11:104778400-104788800	Weak transcription	Pancreas	Pancrea
4	chr11:104779200-104788000	Weak transcription	Fetal Muscle Trunk	muscle
5	chr11:104783800-104788000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
6	chr11:104785600-104788000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
7	chr11:104786000-104788000	Enhancers	Primary B cells from peripheral blood	blood
8	chr11:104786600-104788200	Enhancers	Primary T cells from cord blood	blood
9	chr11:104786800-104787600	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
10	chr11:104786800-104787800	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr11:104786800-104787800	Enhancers	Dnd41	blood
12	chr11:104786800-104788000	Enhancers	Adipose Nuclei	Adipose
13	chr11:104786800-104789400	Flanking Active TSS	HUVEC	blood vessel
14	chr11:104786800-104789800	Active TSS	Aorta	Aorta
15	chr11:104787000-104787600	Weak transcription	Fetal Muscle Leg	muscle
16	chr11:104787000-104787600	Weak transcription	Psoas Muscle	Psoas
17	chr11:104787000-104787800	Enhancers	NHDF-Ad	bronchial
18	chr11:104787000-104788000	Weak transcription	Skeletal Muscle Female	skeletal muscle
19	chr11:104787000-104788200	Weak transcription	Skeletal Muscle Male	skeletal muscle
20	chr11:104787000-104788600	Weak transcription	Left Ventricle	heart
21	chr11:104787000-104788600	Weak transcription	Sigmoid Colon	Sigmoid Colon
22	chr11:104787000-104788600	Weak transcription	Small Intestine	intestine
23	chr11:104787000-104789200	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr11:104787000-104789400	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
25	chr11:104787000-104789600	Active TSS	Primary T cells fromperipheralblood	blood
26	chr11:104787000-104789600	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
27	chr11:104787200-104787800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr11:104787200-104787800	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
29	chr11:104787200-104787800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
30	chr11:104787200-104787800	Enhancers	Rectal Smooth Muscle	rectum
31	chr11:104787200-104788000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
32	chr11:104787200-104788200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr11:104787200-104788400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
34	chr11:104787200-104788400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
35	chr11:104787200-104789400	Active TSS	Ovary	ovary
36	chr11:104787200-104789600	Active TSS	Duodenum Mucosa	Duodenum
37	chr11:104787400-104787600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr11:104787400-104787600	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
39	chr11:104787400-104787600	Flanking Active TSS	Duodenum Smooth Muscle	Duodenum
40	chr11:104787400-104787600	Enhancers	GM12878-XiMat	blood
41	chr11:104787400-104787800	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
42	chr11:104787400-104787800	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
43	chr11:104787400-104788000	Weak transcription	NHLF	lung
44	chr11:104787400-104788200	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
45	chr11:104787400-104788200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr11:104787400-104788200	Enhancers	Colon Smooth Muscle	Colon
47	chr11:104787400-104788400	Enhancers	Primary B cells from cord blood	blood
48	chr11:104787400-104789400	Active TSS	Stomach Smooth Muscle	stomach
49	chr11:104787400-104789600	Active TSS	Rectal Mucosa Donor 29	rectum
50	chr11:104787400-104789600	Active TSS	Right Atrium	heart

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