Variant report

Variant	esv3401646
Chromosome Location	chr11:63529601-63532149
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:11)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr11:63526116..63528464-chr11:63528882..63530638,2	K562	blood:
2	chr11:63532131..63538052-chr11:63579345..63585604,10	K562	blood:
3	chr11:63527527..63531451-chr11:63579707..63582153,3	MCF-7	breast:
4	chr11:63531277..63535286-chr11:63705300..63707994,3	MCF-7	breast:
5	chr11:63438066..63440126-chr11:63528980..63530613,2	MCF-7	breast:
6	chr11:63515783..63518081-chr11:63529282..63531993,2	K562	blood:
7	chr11:63532131..63535124-chr11:63579146..63582872,4	K562	blood:
8	chr11:63528210..63531118-chr11:63540362..63542813,2	MCF-7	breast:
9	chr11:63532069..63539323-chr11:63579489..63583130,14	MCF-7	breast:
10	chr11:63520245..63522926-chr11:63528476..63531329,2	MCF-7	breast:
11	chr11:63522435..63525089-chr11:63529331..63531365,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATL3-1	chr11:63527369-63529844	NONHSAT021901

No data

Variant related genes	Relation type
ENSG00000168005	chromatin interactions
ENSG00000110583	chromatin interactions
ENSG00000184743	chromatin interactions

Extended variants
information (count: 93 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:93 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191372409	chr11:63529605-63529606	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
2	rs372291344	chr11:63529606-63529607	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs80127234	chr11:63529623-63529624	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs551524502	chr11:63529644-63529645	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs549176063	chr11:63529661-63529662	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs370078835	chr11:63529662-63529663	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs571396402	chr11:63529683-63529684	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs576014826	chr11:63529724-63529725	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs533964304	chr11:63529731-63529732	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs546418104	chr11:63529739-63529740	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs550837184	chr11:63529767-63529768	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
12	rs369996742	chr11:63529771-63529772	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
13	rs553728289	chr11:63529784-63529785	Active TSS Weak transcription Genic enhancers Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
14	rs567503465	chr11:63529815-63529816	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
15	rs370179888	chr11:63529853-63529854	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs536161742	chr11:63529865-63529866	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs183118290	chr11:63529884-63529885	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs575257586	chr11:63529917-63529918	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs544225400	chr11:63529922-63529923	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs557814460	chr11:63529937-63529938	Active TSS Weak transcription Genic enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs577757866	chr11:63530011-63530012	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs540819049	chr11:63530057-63530058	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs541481146	chr11:63530093-63530094	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs114204570	chr11:63530142-63530143	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs542969675	chr11:63530151-63530152	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs372221230	chr11:63530152-63530153	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs376493230	chr11:63530158-63530159	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562479244	chr11:63530165-63530166	Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs531312772	chr11:63530210-63530211	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs551432790	chr11:63530215-63530216	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs11551215	chr11:63530231-63530232	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs188815060	chr11:63530232-63530233	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs547526695	chr11:63530248-63530249	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs3016226	chr11:63530291-63530292	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs530426906	chr11:63530297-63530298	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs556162190	chr11:63530305-63530306	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs112097519	chr11:63530308-63530309	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs537838272	chr11:63530319-63530320	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs557777951	chr11:63530453-63530454	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs113710885	chr11:63530467-63530468	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs374039275	chr11:63530468-63530469	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs199676695	chr11:63530478-63530479	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs558790480	chr11:63530479-63530480	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372169641	chr11:63530482-63530483	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs577669668	chr11:63530486-63530487	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534044383	chr11:63530507-63530508	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs554309136	chr11:63530529-63530530	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs574175639	chr11:63530539-63530540	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs543236089	chr11:63530540-63530541	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs2957207	chr11:63530575-63530576	Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Strong transcription Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	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
Autism	22495311	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Non-small cell lung cancer	21385341	CNVD
Intellectual disability	22102821	CNVD
Glioblastoma multiforme	21138945	CNVD
Acute myeloid leukemia	20729466	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Pituitary adenoma	18645599	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Prostate cancer	18632612	CNVD
Glioblastoma multiforme	21080181	CNVD
Smith-Lemli-Opitz syndrome	21572526	CNVD
Multiple myeloma	16461302	CNVD
Cancer	16751803	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Metanephric adenoma	20802469	CNVD
Chordoma	21602918	CNVD
Melanoma	18172304	CNVD
Chordoma	18071362	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21785460	CNVD
Breast cancer	16417655	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Prostate cancer	17217626	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	21045282	CNVD
Breast cancer	21806811	CNVD
Breast cancer	22002566	CNVD
Ductal carcinoma	18381933	CNVD
Retinoblastoma	22278416	CNVD
Breast cancer	20953835	CNVD
oto-dental syndrome	17656375	CNVD
Asthma	21956041	CNVD
Breast cancer	17603634	CNVD
Ovarian neoplasms	16753589	CNVD
Non-small cell lung cancer	20864512	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21509527	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Prostate cancer	18779856	CNVD
Cancer	17160897	CNVD
Breast cancer	17001317	CNVD
Oral squamous cell carcinoma	16619035	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16272173	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Colorectal cancer	16882699	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668395	CNVD
Spinal muscular atrophy	17668395	CNVD
Neonatal seizures	17668395	CNVD
Neonatal seizures	17668391	CNVD
Neuroticism	17667963	CNVD
Cancer	17916600	CNVD
Squamous cell cancer	19047905	CNVD
Multiple endocrine neoplasia type 1	19566914	CNVD
XY sex reversal	17503084	CNVD
Berardinelli-seip congenital generalized lipodystrophy	17668391	CNVD
Maculopathy	17646752	CNVD
Breast cancer	17899364	CNVD
Breast cancer	17157792	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:339 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:63501800-63530000	Weak transcription	Psoas Muscle	Psoas
2	chr11:63509000-63534800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
3	chr11:63511000-63534800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr11:63511200-63529800	Weak transcription	Stomach Mucosa	stomach
5	chr11:63515000-63529800	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr11:63516000-63534800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr11:63516400-63533400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr11:63516400-63534200	Weak transcription	Primary B cells from peripheral blood	blood
9	chr11:63516600-63533800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
10	chr11:63516800-63530000	Weak transcription	Esophagus	oesophagus
11	chr11:63517400-63530000	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr11:63518800-63530000	Weak transcription	Aorta	Aorta
13	chr11:63519400-63534800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
14	chr11:63520400-63533400	Weak transcription	GM12878-XiMat	blood
15	chr11:63521200-63534600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
16	chr11:63521400-63534400	Weak transcription	Primary B cells from cord blood	blood
17	chr11:63521400-63534800	Weak transcription	Primary T helper cells fromperipheralblood	blood
18	chr11:63523400-63532600	Strong transcription	Fetal Thymus	thymus
19	chr11:63523400-63533600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
20	chr11:63523600-63533400	Strong transcription	Dnd41	blood
21	chr11:63523800-63530600	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr11:63525000-63534400	Weak transcription	HSMMtube	muscle
23	chr11:63525400-63529800	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr11:63525400-63530200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr11:63525400-63532000	Weak transcription	Spleen	Spleen
26	chr11:63525600-63530000	Weak transcription	Lung	lung
27	chr11:63525600-63532200	Weak transcription	HepG2	liver
28	chr11:63525800-63529800	Weak transcription	Gastric	stomach
29	chr11:63525800-63534600	Weak transcription	Primary T helper cells PMA-I stimulated	--
30	chr11:63526200-63534600	Weak transcription	Primary T cells fromperipheralblood	blood
31	chr11:63526400-63529800	Weak transcription	Duodenum Mucosa	Duodenum
32	chr11:63526400-63530000	Weak transcription	Rectal Mucosa Donor 31	rectum
33	chr11:63526600-63529800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr11:63526600-63529800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr11:63526600-63530600	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr11:63526600-63534800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr11:63526600-63534800	Weak transcription	Small Intestine	intestine
38	chr11:63527400-63530200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr11:63527400-63530200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
40	chr11:63527400-63530200	Strong transcription	Thymus	Thymus
41	chr11:63527600-63529800	Weak transcription	Brain Cingulate Gyrus	brain
42	chr11:63527600-63529800	Strong transcription	A549	lung
43	chr11:63527600-63530000	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr11:63527600-63533600	Weak transcription	Primary hematopoietic stem cells	blood
45	chr11:63527800-63529800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
46	chr11:63527800-63530000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr11:63528000-63530200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr11:63528000-63530200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
49	chr11:63528000-63534200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
50	chr11:63528000-63534200	Weak transcription	Fetal Kidney	kidney

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