| Tag | Content |
|---|
EnhancerAtlas ID | HS092-38930 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr9:131887640-131888370 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:131888209-131888224 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_35067 | chr9:131886742-131888349 | HeLa | | SE_56625 | chr9:131886557-131888431 | u87 | | SE_68769 | chr9:131888293-131890346 | H9 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr9 | 131887788 | 131888223 | | chr9 | 131888225 | 131888368 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH09I129124 | chr9 | 131886880 | 131890107 |
|
Enhancer Sequence | CTGCCTCAGC CTCCCGAGTA GCTGGGATTA CAGGCGCCCA CCACCACACC CGGCTAATTT 60
TTGTATTTTT AGTAGAGACG GGGTTTCACC ATGTTGGGCA GGCTGGTCTC AAACTCCTGA 120
CCTCAGGTGC TTTGTCCTCC CAAAGTGCTG GGATTGCAGG CGTGAGCTGC TGCGCCCGGC 180
CCAGGTATTG TCTTAGCTCA AGGGCTGTAC TTTGGCAGGA TTGCAGTGTG GTTACATGCT 240
TGGGTTCTGG AGTCCAGCTG GCTAGTTTCA TAACTTGTGA ATCATTTTTG ACCCTCTGTT 300
TCCTCATCTG TAGAGTGGTA AGAGTCAGCA GACTAGTCAT GGCCCCCTGG GGAAAATTCA 360
CTGAGATCCC ACGAGTAGTG GTTGTCTTTT GCATAGCGCC TAACACATAC TAAATAAATA 420
CTTCGATTGT TATTAGCTAT TGTTACCATT AGGCATTAGT CAGTTCTAAT TTTCAATAGT 480
GTTGTTGCAT AGAAAGCTAG CTTTTGGCTG GGCGCGGTGG CTCATGACTG TAATCCTAGC 540
ACCTTGGGAG GCCAAGGCGG GTGAATCATG AGGTCAGGAG TTCAAGACCA GCCTGGCCAA 600
CATGGTGGAA CCCCGTCTCT ACTAAAGATA CAAAAAGTTA GCTGGGCGTG GCGGCAGGCA 660
CCTGTAGTCC CAGCTACTTC GGAGGTGGAG TCAGGAGAAT CCTTTGAAAC CCGGGAGGCG 720
GAGGTTGCAG 730
|
