| Tag | Content |
|---|
EnhancerAtlas ID | HS012-24521 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr8:101455390-101456690 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr8:101455906-101455917 | CTTCTGGGAAA | + | 6.62 |
|
| | Number of super-enhancer constituents: 10 | ID | Coordinate | Tissue/cell |
| SE_18537 | chr8:101453463-101457190 | CD4p_CD25-_Il17-_PMAstim_Th | | SE_19357 | chr8:101453387-101456992 | CD4p_CD25-_Il17p_PMAstim_Th17 | | SE_22743 | chr8:101452080-101458132 | CD8_primiary | | SE_27991 | chr8:101454826-101458796 | Fetal_Intestine | | SE_28830 | chr8:101454704-101458694 | Fetal_Intestine_Large | | SE_32305 | chr8:101455108-101456074 | Gastric | | SE_32305 | chr8:101456155-101456770 | Gastric | | SE_32533 | chr8:101454102-101459783 | GM12878 | | SE_36367 | chr8:101454853-101457864 | HMEC | | SE_62291 | chr8:101421434-101542088 | Tonsil |
|
| | 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 |
| GH08I100441 | chr8 | 101453434 | 101458655 |
|
Enhancer Sequence | AGGAGGACGT GAGACAAGGG ATAGGGAGCT AGTGGCTCTG GCAGTGGCAG AGAGTTGTTC 60
GGGAGAACTT CGGTGGTGGT GGAGGCGGTG AGGATGCTCA GAGCTCATTT GTATGTGTGA 120
ATCATTTGTA AGTTGAGGAT TAGTCAGAGG TTGGCTGCAT TGTTACGGAA ATAGTGGGCT 180
GGGTGTGTGC TCAACCTGAA GCTGTGAGGG CTGAATTTTT TCTCTCCTGG AGACATTGTG 240
AACCACAGAA GGCAAGTCAG CTTTTGGGGG CGAGTTTTAA GTGGAGAAAT ATCTCCTTCT 300
CTAATGCTTG CAGTTGGCTC TGAGGGTTGT GGAAGAAAGA CACAATTTAG AGAACTTATA 360
ACGTCCTTGG CCAGATATGC CCAAAGCCAG GATGTCCCCC TAACAGAAGA AACATAGCAC 420
TCCTTTTGCA GGCTGTTCAC GCAATCACTA AGGACCTCCT AGAGAAGATT TGAAATGTGT 480
TGGGGGCAGG AATTTATCCC AAAGATAACT CAGGGACTTC TGGGAAAGTT TTAATGCCTG 540
TAATGCAGAG AACTCCCAAG CCCCTTGAGT ATAGCAGGGT TGGTAAAAGC CTAAGATTGA 600
CTTTGGTAAG ATAGACATCA AAATAGCAAA AACAAGAACC ATTGTAGAAT TTAAGAGAAG 660
CAAAATAATG TCTTTTCTTG GGGCTAACAC TCCTACCTTA ACTATAGCCC TGGTGGTGTG 720
TTCCCTGTAA TTTTCAGGGT GTCTGACTCT GTGTATGAGA GGCTTCCCAT TTCAGTTTGA 780
CTCTGATATT AGTGGTCCAG CCATAATTGC TGTTCAAATA CTAAGAGGCA GGACAGGGAT 840
GGAATGTTTG ACGTGGGAGT GACATCCATT TATTCATTTC TGTGAATGTA TTAGTGCCAG 900
GTATTTCCTC AGGCCTGTTA TCTCTAATGG TCTTTGGACT AGTTCAACCC TCATTGTTAA 960
GATTAGGAAG GAAGTCATGT TGCCCAAGTT GATTCTGTGG CTGGCAGCAG TTGGGTCTCT 1020
TTCCTTCTTT GGGGAGATCA TCAGTGCAGC AGGGGCTGGG TATAGAATAT TGTGAAGGAG 1080
GCCTCTGAGC ATATAGGAGG CTCTGCACCA GCTTCTGTAG TTGGAGCCTC AGCTTGAGGA 1140
GGCAGTGTGG CCACCGGGGA GGAGCTCGGC TTTCCTCACA CAAATCCATT TCCTAGGTGT 1200
GATCTCAGAC AAGGCCCTTT GCTTCGCTTC TCTTTGAGCC TAGCTTCCCT TGACTGCACA 1260
GTAGAAGCAA TTAAACCTTC CTCACTGGAT TGTGGTGAGG 1300
|
