| Tag | Content |
|---|
EnhancerAtlas ID | HS040-05982 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr11:8853940-8854890 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr11:8854224-8854235 | TTTCCCAGAAG | - | 6.62 | | Stat4 | MA0518.1 | chr11:8854567-8854581 | TTTCCAGGAAGCAG | + | 6.07 | | ZNF263 | MA0528.1 | chr11:8854606-8854627 | GGAGGAGGGCAAACCGGAGGG | + | 6.11 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_30063 | chr11:8853695-8856533 | Fetal_Muscle | | SE_35233 | chr11:8853509-8855230 | HeLa | | SE_37090 | chr11:8846416-8856928 | HSMMtube | | SE_39039 | chr11:8853914-8855463 | IMR90 | | SE_42470 | chr11:8853907-8854899 | Lung | | SE_44642 | chr11:8853912-8856548 | NHDF-Ad | | SE_50316 | chr11:8853909-8854890 | Sigmoid_Colon | | SE_51898 | chr11:8853878-8856577 | Skeletal_Muscle_Myoblast | | SE_54305 | chr11:8853891-8854900 | Spleen | | SE_63676 | chr11:8853280-8856636 | HSMM |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I008829 | chr11 | 8850761 | 8857957 |
|
Enhancer Sequence | GTGGGCCGAG ATTGTGCCAT TGCACTCCAG CCTGGCAACA GAGCGAGACT CTGTCTCCAA 60
AAAAAAAAAA AAAAAAAAGA ACCAACACCT CATCACAATC CATGAAAAGC TAGCTCCTGG 120
CTCTAGGACT GCAAGAAAAG GGAATTCCAC CTTCAAACTC CTGGTTACCT TCCATGGCTG 180
GTCTCAGTGG AACTAGCATT CCTCCTCACA GAGGCATGAG GCAGCCACAC CCCACACAGC 240
CCCAGAGCCC AGAGGCAGAG TTGGGCAGAA AGGAATGCAG ATAGTTTCCC AGAAGTGTCT 300
GGCCGAGAAG GAAACCAAGA GCTTACCCAC AGCTTCCTGG GCCCTGACTG GGAGGCACTG 360
GGTTCTCACA ACAAGGATTC TGGCAATTCA GGGATGGTGA GGCCCTTGTA TGTGAAAGCC 420
CACAGGAGGC GAGGACACAG TGGTGGGAAG AGGCCCTGAC AGAACAAGCC TGGGCTGGCC 480
CCAGACGGCT TCCAGTAAGC AGCGGCTGCA CTTGAATGTC AGCAAGGGTC TTAGGGAGAC 540
CCGAAGCAAT CCAGTCACAG GGGAGCCCAA GGCAGGCACG CAGATGTGAG GTCGGATCCT 600
CTTAGCATAG GCTTTGGCGT CACCTGCTTT CCAGGAAGCA GGCTTCATTT TCTAACACAT 660
CTTGAGGGAG GAGGGCAAAC CGGAGGGGAA GCCCAACATC TGACAGGCCA GCAAAGCTGG 720
TGAGCAGATG GGCTCTAATG CCTCCCAGCT TGATTCTCTC AGTCATGCTT CAGAGGTCAT 780
AAGGCTTTTT TTAGTCCTAC TGTTAGTACC ACAGCTCCCA GAAGCCTGTG CTTCCTCCAA 840
ATTATGACCC TGTAAGGCTC TGTTCTAGGA TAAGCACAGG AGAAGGAGCA GAACACAGAA 900
AGAGTTATTA AAGATGCCTT CCTGTTATAT ACTAAGTGTC CACGTGAAGG 950
|
