| Tag | Content |
|---|
EnhancerAtlas ID | HS187-04556 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr11:66079180-66081950 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr11:66080727-66080745 | GCTTCCTCACCTCCTTCC | - | 6.31 | | KLF16 | MA0741.1 | chr11:66079835-66079846 | GGGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr11:66079836-66079846 | GGGGCGGGGC | - | 6.02 | | KLF5 | MA0599.1 | chr11:66080303-66080313 | GGGGCGGGGC | - | 6.02 | | RREB1 | MA0073.1 | chr11:66081294-66081314 | TCCCCCACCACCCCCAGCCA | + | 6.26 | | SP1 | MA0079.4 | chr11:66079800-66079815 | CAGGGGCGTGGCTTG | - | 6.21 | | SP1 | MA0079.4 | chr11:66080322-66080337 | TGTGGGCGGGGCCTC | - | 6.45 | | SP2 | MA0516.2 | chr11:66081142-66081159 | CTCACCCCCGCCCCCCA | + | 6.3 | | SP4 | MA0685.1 | chr11:66080320-66080337 | TTTGTGGGCGGGGCCTC | - | 6.21 | | SP4 | MA0685.1 | chr11:66079932-66079949 | AGAGGGGGCGGAGCTTG | - | 6.2 | | SP4 | MA0685.1 | chr11:66079687-66079704 | AGTGTGGGCGGGGCGTG | - | 6 | | ZNF263 | MA0528.1 | chr11:66081410-66081431 | TTTCCCATCCCAGCCTCCTCC | - | 6.09 | | ZNF263 | MA0528.1 | chr11:66080589-66080610 | CCTTCCCCACTCCCATCCCCC | - | 6.1 |
|
| | Number of super-enhancer constituents: 14 | ID | Coordinate | Tissue/cell |
| SE_17595 | chr11:66078577-66087464 | CD4p_CD25-_CD45RAp_Naive | | SE_21742 | chr11:66078997-66086804 | CD8_Naive_7pool | | SE_22096 | chr11:66078856-66087270 | CD8_Naive_8pool | | SE_23038 | chr11:66078869-66087217 | CD8_primiary | | SE_30998 | chr11:66078967-66082451 | Fetal_Thymus | | SE_39117 | chr11:66080439-66086908 | IMR90 | | SE_44309 | chr11:66079188-66080240 | NHDF-Ad | | SE_44309 | chr11:66080385-66086883 | NHDF-Ad | | SE_44843 | chr11:66079177-66080267 | NHLF | | SE_44843 | chr11:66080506-66086616 | NHLF | | SE_46566 | chr11:66079130-66087048 | Osteoblasts | | SE_50962 | chr11:66078995-66086930 | Sigmoid_Colon | | SE_55281 | chr11:66079268-66081500 | Thymus | | SE_55281 | chr11:66081616-66082216 | Thymus |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | AGATTGTCAG GGGCGCTCAG CTCATAGGGT GGCTCGAGGG CCAGTGCGAA GCTCCCTTAG 60
GGACGAATTT CCACATACGA CGAAAGGCAT CTGCGAAAGG ATGGGCTGTC CCGTGGGGGG 120
AGTCGGCAGA TATTTAAGTA ACACTAACAT TTAACGAATT AAGCAGCTAT TTCTATTTAC 180
TGAGCAATTA GTACGCTTTG AGAGAGAGGC CCTACCGAGG CCTCGCGGTG GCTGTAAGTC 240
CGTGGGGCCG AGGCCAGGTG GCGCCAAAGG CCCATCGACG CCATCTGCCC GGCTGTCCGG 300
GCCCAGTCTC CGGGCTCGCC CAGAGAACCC GAAATCTGGA CAAACGGAAA CCGTAGGTGG 360
AGGAAGAAGA GGGCTCCAGG GCCAGGTTCA AGGGCATCGT GGTGAGAGAT GAGGGGTTCG 420
GAGGACTGGT GGATCTGGGC ATATCGCGAA GGTGGTAAGG GACCCAGGGG TGGAGTGGGC 480
GGTGCTTGCG CCAAGAGGGT GAGCCTGAGT GTGGGCGGGG CGTGCGATAA GAGGCTCGCT 540
CGGTAGCGCT CTTCGCAGAG CCGTATTTGT GCGCTACGCC GCAGCCAGGG CGCTCTGGGT 600
GGGCGGGACT CCAGGGCCCC CAGGGGCGTG GCTTGCATCT TTCGTGGGCG GCCCCGGGGG 660
CGGGGCTCCG TGTAGGTGAA CCGCTACCTC CGCTCGATGT GTGAGGTGTG ACAGTCCTAC 720
GAGGGCGCAG TTCTTCCACT TTTGTGAGCT TGAGAGGGGG CGGAGCTTGT AGCTGGGGAC 780
GGAGCCTGAA GAGGAGGTTG AGGGGAACTT CACACGTTTC CCTGGAGGGC GGAGTTTACA 840
TCATCCCCCA ACAGAGTTAA GACCTCTGAG GGATTCCCTG CAGTGTCCAG GGCTCTGTGA 900
GGCGAAGCTT GCAGTTGTGT TGGGCGGGGC CTGTAGCGCC GCGTGAAGAG AATGTGTAAA 960
CTCGGGGCGA AGTTCATACC TCCTAGAAGC CGAGACTAAT AGTTCCGCCA ATCTGCGCGC 1020
GCCGAGCGGA GGAGGTGGGG CTTGTAGGTT GTGGGCGGGG GACTGGGCGG GGCCAAGAGG 1080
GCAGGGGGCG GGCACAATCG CTGCTGGAAT CTTTGAGTTG GCAGGGGCGG GGCTTGTGGC 1140
TTTGTGGGCG GGGCCTCTGG AGAGCTCCCG GGGGCTCTCT TCTGTTCTGC AGCGAGTAGG 1200
CGTGGCTCGT AGCTCCCAGG TCCGGGCTGA TACCGCTGGA GTATGCAGTT CGCCGCCGCG 1260
CCCGAATGAG GCGGGGCCTG CGAGTAAGTG GGCTGAGCCC GGGCTGGGCG CAGGCCGGGG 1320
CTCTGCCCTG GGAGGCCGTC TGTTTAGGCC CGCACGCAGC TCCGCATCTG GTGCTCATTA 1380
CCAGATGACA AAGAGCCGGC TCTGGGCCCC CTTCCCCACT CCCATCCCCC GCCTCCGACT 1440
GCAGTGTATT TAACTGTTTC CTGCCCTCGA GGCGCTCTAG ATCCCTACCC GAGGTCACGG 1500
AGGGGACTCC AGACCATCCC GTCTCTGCAG GCCTTGTCGC TCCCCAGGCT TCCTCACCTC 1560
CTTCCCAGAC TCAGCCGTCT GGGCCGCCTC GCAACCCTCA TTGGCATCCA GCAAACCTGC 1620
CCGACGGCGT CTCCGAGGTT AAAGCTGTGC AGGATCTGGC GGGGACGTCT GGTTTGAGTT 1680
AGGGGAACGT GAGAGCGGGG ACCGGGGGCG GTGCGTAGCG TTCCCTCCGC CCCCTCCGCG 1740
ACCCCCTGGT TCATCCCCAG CTCCGGCCCC TCCTTTCCTG GTTCCCTGGG GCCCAGCTCA 1800
GCCTTCCAGC TCAGGTCCAG GCCCGAAGGG GGCGCTGGGC CACTCCTCCT CGCCTGCCCG 1860
GGTGGTCGTG GCGGCTCTGC CCCGTCCTAA TTAGAGGCCC CCAAGAGGCT GTAACTGAAA 1920
AATTACAGAG GCGGTGGGAA CTGGCGCCTC CCCTCCCCAG GTCTCACCCC CGCCCCCCAA 1980
GGCAGTGAGC ACGAAATGAG GGAGGTCACT CCCACCAGGC TGTGATCTTT GACCAGGCCC 2040
TCCAGTTCCT GGGACACTTC AGTCCTGAGC AGCCGGAGCC CTCGCTCAAG CTCAGGTCTG 2100
CTGAGCTCTG TCTGTCCCCC ACCACCCCCA GCCAACATGG ACAAGAGCAA CGTGCGGCCC 2160
TGGCAAAAGG AGGCCTTGCT CCTGCGGCTG TCCAAGCAGT TAGCATGGGA TCTCTCCCAG 2220
GTTCCCGGCC TTTCCCATCC CAGCCTCCTC CCCGGAGCAA GCGGAGGAAT GCCTCCAAGA 2280
GCACCCACAA ACCAGGGGTT GGCAGTCCCC TTGAGTTACC CTGAGCCCCA GCCCCCAACT 2340
TCCGCGAAGC TTACAGGGAT GGGAAGGGAA GTGTCTGAAG AAAGGAGCAA CTCACCCACT 2400
AGACCCCTCC TTCACTCCTC TGAATCACCA GCCCCAGAGC CTACTTTGAC CCCTAAACCC 2460
CAGTCCGGTT CAGCAGATGC CCTAATTCCA CAACCGTCCC CCAGATTCAG CCCCACCTTC 2520
TTGGAGCTTT GGTAAAATAA GGAATAAATA TGAAATTCTC CCCATGCCAA ACCTCCCACT 2580
GCTGGGCTCA ACTGTGTGAC CTTGGGCAAG GCTCTGCCCT CTCTGGGCTC CTGCTTCCCT 2640
GAGAATCTCT GAGGCATACC CTCCCTTAAA GGGATCTTAC CTTATCTCTT TGAGGACTCA 2700
GACAAACTGA AGGAAGATCC CCTCCTTTTT GCTGAGTCCT CCCAGAACCT CCCTTAAGCA 2760
CCAGTGGGGG 2770
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