| Tag | Content |
|---|
EnhancerAtlas ID | HS053-00775 |
Organism | Homo sapiens |
Tissue/cell | Foreskin_keratinocyte |
Coordinate | chr1:27193270-27194750 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TP53 | MA0106.3 | chr1:27193597-27193615 | GGCATGCACCAGCATGTC | - | 6.13 | | TP53 | MA0106.3 | chr1:27193597-27193615 | GGCATGCACCAGCATGTC | + | 6.17 |
|
| | Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
| SE_26621 | chr1:27193611-27195235 | Esophagus | | SE_34025 | chr1:27193917-27194938 | HCC1954 | | SE_34526 | chr1:27193835-27194826 | HCT-116 | | SE_64263 | chr1:27194021-27194814 | NHEK |
|
| | 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 |
| GH01I026867 | chr1 | 27193925 | 27194757 |
|
Enhancer Sequence | CTGCCTCAGC CTCCCGTGTA GCTGGGACTA CAGGCGCGCG CCACCATGCC CGGCTAATTT 60
TTGTATTTTT AGTAGAGACG GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA 120
CCTCGTGATC CGCCCGTCTC GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGCCACCGC 180
GCCCGGCCTA TTTTGTTTAT TTTTATATGG AGTCTCGCTC TGTTGCCCAG GCTGGAGTGC 240
AGTGGTGCAA TCTCGGCTCA CTGCAACCTC TGCCTCCTGG GTTCAAGCGA TTCTCCTGCC 300
TCAGCCTCCT TAGTAGCTGG GATTACAGGC ATGCACCAGC ATGTCCAGCT AATTTTTTGT 360
ATTTTTAGTA GAGACGGGGG TTTCACCATG TTGGTCAGGC TGGTCTCGAA CTCCTGACCT 420
CGTGATCCAC CCACCTTGGC CTCCCAAAGT GCTGGGATTA CAGGCGTGAG CCACCACACC 480
CGGCCTATTT TTTATTTATT TTTTATTTTT TATTTTTGAG ACAGGGTCTG GCTCTGTCAC 540
CCCAGGCGTG ACAGTGGCTT TTGGTCTCAA GCAATCCTCC CACCTCAGCC TCCTGGTAGC 600
TGGGACTATA GGTGCCTGCC ACCGCACCCA GCTAATTTTT TATTTTATTT TTAGTAGAGA 660
CAAGGTTTCA CCATGTTGGC CAGACTGGTC TCAAACTCCT GGGCTCAAGC GATCCTCCTG 720
CCTCAGCTTC CCAAAGTGCT AGGGTTACAG GCTTGTGCCA CCTCACCCAG CCTCAAATGT 780
CAGCTATTAA CGAATCCTTC CAGCTTCAAT AAGTCTAGGA TTTGGCCAGC ATTTTTATGC 840
CTAAAGCAGA ATCATGAGGC AGGCCCAGTC CTGAGGGGCA GCCTTATTGC CAAAGCTGAC 900
CTGCACGCCT GCTGAGCCCC CTGAGAATGC TGCCCTCACA TCAGGTGGTC ACTCTTCCAC 960
CTGGCAAGAT GGAGAGAGCT AAGCCCAGGG TCCAAGCTTG GCCACACCAA TAGGACTCAA 1020
AACTGAAGGG TTTTTGTCAG AACTCCTGCT TCTACAGGGG AAGCCGGCAG GACCACTCTG 1080
ATGCCTTCTG GGTCCCCTGT TTTCTCCCTT CCTTTCCTAG AGGTGTGTCA GATTTCAAGG 1140
CTCCAAACCA GGGACTCTAG GCAGGGCAAG TAACTCCACT CAGATCTAGA GGTGACCTGA 1200
TTTCTCTCAC CAGACAGGTC TGGTGACTCT CTCTTAATGG GCTACATCCT GGGAAAGGAA 1260
CTTCTTTCTT TTCTCTCAGC CTCTGACTTT TGTCTGTTAG CTCTGGACCA CTCGTGGTTG 1320
TCCCATATGG GGAGAAGTGA GCTGCCCTAA GGTAGTGTGT CGGTGTAAGG ATTTTAAACC 1380
AGATGCTGTG CATTGGAATA TCTCTAAATC AGATGCTTAC CAGGGCTAAA TGTGAGCTGG 1440
CTTAGGCACC AGCTTCTTTT ATTTTCTTTT CTCTCTCTCT 1480
|
